|
rs1044250
|
ANGPTL4
T266M
|
Protective missense variant that reduces LPL inhibition, lowering fasting tri...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs1044317
|
ABCG1
ABCG1 3'UTR variant
|
3'UTR variant in ABCG1 that may reduce transporter expression, impairing chol...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs10455872
|
LPA
|
Intronic variant strongly associated with elevated lipoprotein(a) levels and ...
|
Atherogenic Lipoproteins
|
|
Established
|
|
rs10846744
|
SCARB1
|
Intronic SCARB1 variant associated with altered HDL-receptor function, subcli...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs11591147
|
PCSK9
R46L
|
Loss-of-function variant that naturally lowers LDL cholesterol by 15-28% and ...
|
Atherogenic Lipoproteins
|
|
Established
|
|
rs116843064
|
ANGPTL4
ANGPTL4 E40K
|
Missense variant that reduces ANGPTL4's inhibition of lipoprotein lipase, low...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs1148259
|
ANKRD30A
|
Synonymous variant in the 3′ UTR of ANKRD30A associated with altered circulat...
|
Metabolic Enzymes & Rare Disorders
|
|
Emerging
|
|
rs11857380
|
LIPC
|
Intronic LIPC variant tagging reduced hepatic lipase expression; G allele ass...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs12487736
|
SCAP
SCAP Val798Ile
|
Missense variant in the SCAP cholesterol-sensor gene (Val798Ile); the C allel...
|
Atherogenic Lipoproteins
|
|
Moderate
|
|
rs10515522
|
NR3C1
|
Intronic NR3C1 variant associated with longevity in Polish nonagenarians and ...
|
Longevity & Aging
|
|
Emerging
|
|
rs12593008
|
LIPC
|
Intronic LIPC variant in intron 1 associated with low HDL risk, predominantly...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs12785878
|
DHCR7
Near gene T>G
|
Influences vitamin D synthesis by regulating how much 7-dehydrocholesterol is...
|
Vitamin D Metabolism
|
|
Strong
|
|
rs137852912
|
PCSK9
D374Y
|
The most severe gain-of-function PCSK9 mutation, increasing LDLR-binding affi...
|
Atherogenic Lipoproteins
|
|
Established
|
|
rs1125226
|
CYP7A1
CYP7A1 upstream promoter variant
|
Upstream regulatory variant in CYP7A1 that tags haplotypes affecting bile aci...
|
Cholesterol & Lipoproteins
|
|
Emerging
|
|
rs137853964
|
LDLR
Val827Ile / Val827Phe
|
LDLR missense variant at position 827 within the cytoplasmic NPXY internaliza...
|
Atherogenic Lipoproteins
|
|
Moderate
|
|
rs11568822
|
APOC1
APOC1 HCR-1 promoter variant
|
Promoter insertion variant in APOC1 that increases gene transcription by 50%,...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs1378577
|
ABCG1
ABCG1 ischemic stroke variant
|
Regulatory variant ~2kb upstream of ABCG1 that modulates transporter expressi...
|
Atherogenic Lipoproteins
|
|
Moderate
|
|
rs1800588
|
LIPC
-514C>T
|
Promoter variant that reduces hepatic lipase activity, raising HDL-C levels b...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs121918383
|
APOB
APOB Arg1333Ter
|
Nonsense mutation in APOB creating a premature stop codon at position 1333, t...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs12740374
|
SORT1
1p13.3 locus
|
Regulatory variant that increases sortilin expression, lowering LDL cholester...
|
Coronary Artery Disease & Atherosclerosis
|
|
Established
|
|
rs121918384
|
APOB
APOB Val1856fs
|
Frameshift deletion in APOB causing truncated apolipoprotein B-100, reducing ...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs121918393
|
APOE
Christchurch (R136S)
|
Ultra-rare APOE3 missense variant that dramatically reduces HSPG binding and ...
|
Longevity & Aging
|
|
Strong
|
|
rs1532085
|
LIPC
|
Intronic eQTL that reduces hepatic lipase expression, raising HDL-C levels wh...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs186021206
|
ASGR1
|
Intergenic tag SNP 7.3 kb downstream of ASGR1; the rare A allele proxies the ...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs2228603
|
NCAN
T130M (Pro92Ser)
|
Missense variant in neurocan associated with hepatic steatosis, liver inflamm...
|
Liver Fat
|
|
Moderate
|
|
rs121918385
|
APOB
APOB Glu4034fs
|
Frameshift deletion in APOB that truncates apolipoprotein B, causing familial...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs121918386
|
APOB
APOB Arg2085Ter
|
Nonsense mutation in APOB creating a premature stop codon at position 2085, p...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs17301739
|
LIPC
|
Intronic LIPC variant associated with circulating DHA and omega-3 fatty acid ...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs2642438
|
MTARC1
p.Ala165Thr (A165T)
|
Protective missense variant that reduces MTARC1 protein stability, cutting he...
|
Liver Fat
|
|
Established
|
|
rs28942111
|
PCSK9
S127R
|
Gain-of-function PCSK9 missense variant (Ser127Arg) causing autosomal dominan...
|
Atherogenic Lipoproteins
|
|
Established
|
|
rs121918387
|
APOB
ApoB-67 frameshift
|
Single-nucleotide deletion in APOB creating a truncated apolipoprotein B (Apo...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs17321515
|
TRIB1
|
Near-gene variant 30–44 kb downstream of TRIB1; A allele raises triglycerides...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs3798220
|
LPA
Ile4399Met (I4399M)
|
Missense variant in the protease-like domain of apolipoprotein(a) causing mar...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs121918388
|
APOB
APOB Q2279X
|
Nonsense variant creating a premature stop codon at amino acid 2279 of apolip...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs3829251
|
NADSYN1
|
Intronic NADSYN1 variant at the DHCR7/NADSYN1 vitamin D locus; A allele was t...
|
Vitamin D Metabolism
|
|
Strong
|
|
rs4149338
|
ABCA1
ABCA1 3'UTR Stroke-Associated Variant
|
3'UTR variant in the ATP-binding cassette transporter A1 gene; the G allele (...
|
Atherogenic Lipoproteins
|
|
Emerging
|
|
rs121918389
|
APOB
Q1477X (apoB-32)
|
Nonsense mutation producing a severely truncated apolipoprotein B (apoB-32) t...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs121918390
|
APOB
APOB R2522X
|
Nonsense mutation truncating apolipoprotein B at residue 2522, causing famili...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs1333049
|
CDKN2B-AS1
9p21 locus
|
Strongest GWAS signal for coronary artery disease; risk C allele accelerates ...
|
Longevity & Aging
|
|
Established
|
|
rs121918391
|
APOB
APOB Tyr1200Ter
|
Rare APOB stop-gain variant that truncates apolipoprotein B to ~27% of its fu...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs505151
|
PCSK9
E670G
|
Common missense variant in PCSK9 exon 12 where the rare G allele raises LDL c...
|
Atherogenic Lipoproteins
|
|
Moderate
|
|
rs12447924
|
CETP
|
Upstream promoter variant in CETP that tags the HDL-raising haplotype block —...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs5128
|
APOC3
3238C>G (SstI)
|
Regulates triglyceride metabolism through effects on APOC3 expression in the ...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs58542926
|
TM6SF2
E167K
|
Lipid transport variant that impairs VLDL secretion, creating a paradoxical t...
|
Liver Fat
|
|
Strong
|
|
rs12686004
|
ABCA1
|
Intronic ABCA1 variant associated with population differences in HDL choleste...
|
Cholesterol & Lipoproteins
|
|
Emerging
|
|
rs12713559
|
APOB
APOB R3558C
|
Rare APOB missense variant reducing LDL-receptor binding affinity by ~40-50%,...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs137943601
|
LDLR
LDLR E408* (Glu408Ter)
|
Nonsense mutation in the LDLR gene creating a premature stop codon at positio...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs20455
|
KIF6
Trp719Arg
|
Missense variant in kinesin family member 6; the Arg allele was associated wi...
|
Coronary Artery Disease & Atherosclerosis
|
|
Moderate
|
|
rs55714927
|
ASGR1
ASGR1 K89K
|
Synonymous coding variant (Lys89Lys) in the asialoglycoprotein receptor 1 gen...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs7940244
|
NADSYN1
Near DHCR7
|
Intronic NADSYN1 variant in the DHCR7/NADSYN1 vitamin D locus; T allele tags ...
|
Vitamin D Metabolism
|
|
Strong
|
|
rs1457043
|
CYP7A1
|
Intronic variant in CYP7A1 that tags a haplotype block influencing cholestero...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs5925
|
LDLR
LDLR Expression Co-variant
|
Synonymous variant in LDLR exon 13 that modulates mRNA splicing efficiency in...
|
Atherogenic Lipoproteins
|
|
Moderate
|
|
rs7944926
|
DHCR7
|
Near-gene intronic variant in the DHCR7/NADSYN1 locus on chromosome 11 that t...
|
Vitamin D Metabolism
|
|
Strong
|
|
rs1800206
|
PPARA
Leu162Val (L162V)
|
Missense variant in PPARA that reduces receptor transcriptional activity, ele...
|
Fitness & Body
|
|
Moderate
|
|
rs1800775
|
CETP
-629C>A
|
CETP promoter variant that reduces CETP expression via Sp1/Sp3 repression, ra...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs185392267
|
PCSK9
Arg96Cys
|
Gain-of-function missense variant in PCSK9 that increases intracellular LDL r...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs6511720
|
LDLR
Intron 1
|
Common regulatory variant in the LDL receptor gene affecting LDLR expression,...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs2228314
|
SREBF2
SREBF2 G1784C
|
Missense variant in the master cholesterol transcription factor SREBP-2 that ...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs2234714
|
ABCG1
ABCG1 promoter variant
|
Intronic ABCG1 variant near the promoter region; homozygous carriers of the m...
|
Cholesterol & Lipoproteins
|
|
Emerging
|
|
rs688
|
LDLR
Asn591Asn (c.1773C>T)
|
Synonymous LDLR variant that disrupts exon 12 splicing, reduces LDL receptor ...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs2249891
|
ABCA1
|
Intronic ABCA1 variant associated with lower HDL-cholesterol susceptibility a...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs693
|
APOB
XbaI (C/T)
|
Silent variant affecting LDL particle number and lipid metabolism; A allele c...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs2575876
|
ABCA1
|
Intronic ABCA1 variant associated with HDL-C levels under a recessive model; ...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs708272
|
CETP
TaqIB
|
Influences HDL cholesterol levels and particle size through effects on choles...
|
Atherogenic Lipoproteins
|
|
Strong
|
|
rs2000813
|
LIPG
|
Missense variant in endothelial lipase that tags a regulatory haplotype assoc...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs2853579
|
ABCA1
|
Synonymous coding variant in ABCA1 that tags a regulatory element influencing...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs28942083
|
LDLR
Cys667Tyr
|
Pathogenic LDLR missense variant abolishing LDL receptor surface expression, ...
|
Cholesterol & Lipoproteins
|
|
Established
|
|
rs730882105
|
LDLR
p.Val524Met
|
Rare LDLR missense variant (c.1570G>A, p.Val524Met) associated with familial ...
|
Atherogenic Lipoproteins
|
|
Moderate
|
|
rs2073658
|
USF1
USF1 FCHL Variant
|
Intronic USF1 variant; the T allele disrupts insulin-responsive USF1 regulati...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs28942084
|
LDLR
LDLR Pro685Leu
|
Pathogenic LDLR missense variant in the EGF precursor domain causing familial...
|
Cholesterol & Lipoproteins
|
|
Established
|
|
rs763625913
|
LDLR
Q770* (c.2308C>T)
|
Rare pathogenic nonsense variant in the LDL receptor gene that abolishes rece...
|
Atherogenic Lipoproteins
|
|
Established
|
|
rs28942085
|
LDLR
LDLR Y828C (J.D. mutation)
|
Pathogenic LDLR missense variant (p.Tyr828Cys) that traps LDL receptors outsi...
|
Cholesterol & Lipoproteins
|
|
Established
|
|
rs2197089
|
LPL
LPL Regulatory Variant
|
Downstream regulatory variant affecting LPL expression and triglyceride clear...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs3846662
|
HMGCR
HMGCR Intron 13 Splice Variant
|
Intronic HMGCR variant that modulates alternative splicing of exon 13, produc...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs3846663
|
HMGCR
HMGCR Exon 13 Haplotype Tag
|
Intronic HMGCR variant that tags a haplotype influencing exon 13 alternative ...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs2278236
|
ANGPTL4
ANGPTL4 Intronic Variant
|
Intronic ANGPTL4 variant tagging reduced LPL inhibition; the A allele is asso...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs4149268
|
ABCA1
|
Intronic ABCA1 variant — the C allele tags a liver enhancer that boosts ABCA1...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs4977574
|
CDKN2B-AS1
9p21.3
|
Independent 9p21.3 CAD risk signal in ANRIL; G allele elevates coronary arter...
|
Coronary Artery Disease & Atherosclerosis
|
|
Established
|
|
rs4149274
|
ABCA1
|
Intronic ABCA1 variant influencing HDL-cholesterol levels through altered ABC...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs264
|
LPL
LPL Intron 6 Variant
|
Intronic LPL variant associated with altered triglyceride clearance and HDL l...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs429358
|
APOE
E4 determinant
|
Lipid metabolism and Alzheimer's risk - E4 carriers respond worse to high sat...
|
Cholesterol & Lipoproteins
|
|
Established
|
|
rs4783961
|
CETP
|
CETP promoter variant that raises HDL cholesterol by reducing cholesteryl est...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs4900442
|
CYP46A1
|
Intronic variant in the brain cholesterol 24-hydroxylase gene; C allele assoc...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs662
|
PON1
Q192R
|
Affects paraoxonase-1 enzyme activity for detoxifying organophosphates and pr...
|
Vascular Inflammation & Remodeling
|
|
Moderate
|
|
rs2854116
|
APOC3
T-455C
|
APOC3 promoter variant that disrupts insulin suppression of ApoC-III, raising...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs520354
|
APOB
APOB IVS6+360
|
Intronic APOB variant where the A allele (plus strand) is associated with app...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs2854117
|
APOC3
APOC3 C-482T
|
Promoter variant in APOC3 disrupting insulin-responsive regulation of apolipo...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs5888
|
SCARB1
|
Synonymous variant that reduces SR-BI receptor expression and impairs HDL cho...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs2918418
|
NR3C1
|
Intronic NR3C1 variant with CC genotype enriched in Polish centenarians; GG g...
|
Longevity & Aging
|
|
Emerging
|
|
rs606231236
|
APOB
|
Pathogenic APOB splice acceptor variant causing familial hypobetalipoproteine...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs7566605
|
INSIG2
|
Upstream regulatory variant near INSIG2 that influences lipogenesis control a...
|
Appetite & Obesity
|
|
Moderate
|
|
rs2954021
|
TRIB1
|
Near-gene variant influencing hepatic lipid metabolism; G allele raises trigl...
|
Triglycerides & Fatty Acids
|
|
Established
|
|
rs2963154
|
NR3C1
|
Intronic NR3C1 variant with TT genotype enriched in Polish centenarians; C al...
|
Longevity & Aging
|
|
Emerging
|
|
rs673548
|
APOB
|
Intronic APOB variant associated with modest differences in apolipoprotein B ...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs854571
|
PON1
PON1 -108C>T promoter variant
|
Promoter variant that controls PON1 transcription; the T allele reduces PON1 ...
|
Vascular Inflammation & Remodeling
|
|
Strong
|
|
rs3211867
|
CD36
|
Intronic CD36 variant that reduces CD36 expression, impairing postprandial fa...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs854572
|
PON1
PON1 promoter -909G>C
|
Promoter polymorphism that modulates PON1 gene expression level — the G allel...
|
Vascular Inflammation & Remodeling
|
|
Moderate
|
|
rs7412
|
APOE
E2 determinant
|
APOE E2 variant - generally protective for cardiovascular health
|
Cholesterol & Lipoproteins
|
|
Established
|
|
rs35136575
|
APOC1P1
HCR-2 Enhancer Variant
|
Regulatory variant in the APOE/APOC hepatic enhancer HCR-2 that lowers plasma...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs8192870
|
CYP7A1
CYP7A1 intron 1 variant
|
Intronic variant in the rate-limiting bile acid synthesis gene; T allele carr...
|
Cholesterol & Lipoproteins
|
|
Moderate
|
|
rs3816873
|
MTTP
MTTP I128T
|
Missense variant in MTTP (microsomal triglyceride transfer protein) at residu...
|
Fat Storage & Energy
|
|
Moderate
|
|
rs838880
|
SCARB1
|
3' UTR variant in SCARB1 that tags a haplotype with reduced SR-BI expression ...
|
Cholesterol & Lipoproteins
|
|
Strong
|
|
rs2943641
|
IRS1
Near-gene C>T
|
Regulates insulin signaling efficiency and cellular glucose uptake
|
Blood Sugar & Diabetes
|
|
Strong
|
|
rs3829462
|
LIPC
|
Missense variant in hepatic lipase encoding p.Phe356Leu; the rare C allele (P...
|
Triglycerides & Fatty Acids
|
|
Emerging
|
|
rs5882
|
CETP
I405V
|
Missense variant that reduces CETP enzyme activity, raising HDL-C and enlargi...
|
Longevity & Aging
|
|
Moderate
|
|
rs3487348
|
PTPN1
PTPN1 LD Block Co-Variant
|
Intronic PTPN1 variant in the 100-kb haplotype block; T allele associated wit...
|
Blood Sugar & Diabetes
|
|
Moderate
|
|
rs4148102
|
ABCG1
ABCG1 intronic PUFA-interaction variant
|
Intronic variant in the ABCG1 cholesterol efflux transporter gene that modifi...
|
Triglycerides & Fatty Acids
|
|
Emerging
|
|
rs4775065
|
LIPC
|
Intronic LIPC variant associated with susceptibility to low HDL-C and coronar...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs5181
|
LRP8
Trp466Cys
|
Rare missense variant in the ApoE receptor 2 (LRP8) ligand-binding domain, di...
|
Fat Storage & Energy
|
|
Emerging
|
|
rs4939883
|
LOC105372112
|
Intronic variant near LIPG whose T allele increases circulating endothelial l...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs5082
|
APOA2
-265T>C
|
Promoter variant that reduces APOA2 expression by 30%; GG homozygotes consumi...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs57137919
|
ABCG1
|
ABCG1 promoter variant that reduces transporter expression, impairing macroph...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs5956
|
CD36
|
Synonymous coding variant in CD36 fatty acid translocase; the minor A allele ...
|
Triglycerides & Fatty Acids
|
|
Emerging
|
|
rs6507931
|
LIPG
|
Intronic LIPG variant that modulates HDL cholesterol levels, with strongest e...
|
Triglycerides & Fatty Acids
|
|
Moderate
|
|
rs692383
|
ABCG1
ABCG1 HDL-c Variant
|
Intronic variant in the ABCG1 cholesterol efflux transporter gene associated ...
|
Triglycerides & Fatty Acids
|
|
Emerging
|
|
rs8034802
|
LIPC
|
Intronic LIPC variant associated with higher baseline HDL-C and an amplified ...
|
Triglycerides & Fatty Acids
|
|
Emerging
|
|
rs964184
|
ZNF259
ZNF259/BUD13 Triglyceride Variant
|
Common regulatory variant at the APOA5-ZNF259 locus; G allele reduces ApoAV p...
|
Triglycerides & Fatty Acids
|
|
Strong
|
|
rs9951026
|
LIPG
|
Intronic LIPG variant that tags a haplotype associated with higher LDL choles...
|
Triglycerides & Fatty Acids
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Moderate
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rs6017340
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HNF4A
HNF4A Regulatory Variant
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Intronic HNF4A tag SNP associated with altered bile acid synthesis regulation...
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Blood Sugar & Diabetes
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Emerging
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rs6067484
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PTPN1
PTPN1 rs6067484
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Intronic PTPN1 tag SNP within the 100-kb T2D-risk haplotype block — carriers ...
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Blood Sugar & Diabetes
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Moderate
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