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rs10156191
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AOC1
Thr16Met
|
DAO structural variant affecting enzyme activity and histamine degradation
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Methylation & Detox
|
|
Strong
|
|
rs1049742
|
AOC1
|
Missense variant in the diamine oxidase enzyme that contributes to reduced hi...
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Methylation & Detox
|
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Moderate
|
|
rs1049793
|
AOC1
His645Asp
|
DAO structural variant near the catalytic domain affecting histamine degradation
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Methylation & Detox
|
|
Strong
|
|
rs11204971
|
FLG
FLG locus regulatory variant
|
Regulatory tag SNP in the filaggrin (FLG) locus associated with reduced FLG e...
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Allergy & Atopic Disease
|
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Moderate
|
|
rs150597413
|
FLG
S3247X
|
Nonsense variant eliminating filaggrin protein — a minor European FLG null al...
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Skin & Eyes
|
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Strong
|
|
rs12934922
|
BCO1
Arg267Ser
|
Reduces beta-carotene to retinol (vitamin A) conversion efficiency, contribut...
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Vitamins & Nutrient Absorption
|
|
Strong
|
|
rs145946881
|
MCM6
-14010G>C
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African lactase persistence variant — MCM6 enhancer SNP that controls LCT exp...
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Vitamins & Nutrient Absorption
|
|
Strong
|
|
rs397507563
|
FLG
3702delG
|
Frameshift deletion in the third filaggrin repeat domain — the third most com...
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Skin & Eyes
|
|
Established
|
|
rs558269137
|
FLG
2282del4
|
Frameshift deletion eliminating filaggrin protein, the second most common Eur...
|
Skin & Eyes
|
|
Established
|
|
rs61816761
|
FLG
R501X
|
Nonsense variant eliminating filaggrin protein, the major genetic risk factor...
|
Skin & Eyes
|
|
Established
|
|
rs1295686
|
IL13
IL-13 Atopy Promoter Variant
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Intronic variant in IL13 that tags the atopic risk haplotype; the minor T all...
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Allergy & Atopic Disease
|
|
Strong
|
|
rs370793608
|
ALDOB
ALDOB Y204X
|
Nonsense variant in the aldolase B gene creating a premature stop codon at po...
|
Metabolic Enzymes & Rare Disorders
|
|
Established
|
|
rs41380347
|
MCM6
G-13915T
|
East African lactase persistence allele — MCM6 enhancer SNP that independentl...
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Vitamins & Nutrient Absorption
|
|
Strong
|
|
rs17612852
|
HLA-DQA1
HLA-DQA1 Peanut Allergy Tag SNP
|
Intronic tag SNP in HLA-DQA1 in strong LD with HLA-DQA1*01:02; the G allele i...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs601338
|
FUT2
W143X (Trp143Ter)
|
Determines secretor status — whether ABO blood group antigens are secreted in...
|
Vitamins & Nutrient Absorption
|
|
Established
|
|
rs6420424
|
BCO1
|
Upstream regulatory variant near BCO1 that reduces beta-carotene to vitamin A...
|
Vitamins & Nutrient Absorption
|
|
Moderate
|
|
rs2052129
|
AOC1
promoter variant
|
Histamine breakdown in gut - reduced activity means dietary histamine accumul...
|
Methylation & Detox
|
|
Strong
|
|
rs7834555
|
BCO1
|
Intergenic GWAS tag SNP near the BCO1 pathway, associated with circulating be...
|
Vitamins & Nutrient Absorption
|
|
Emerging
|
|
rs4684059
|
HRH1
|
Intronic variant in the histamine H1 receptor gene associated with altered re...
|
Methylation & Detox
|
|
Emerging
|
|
rs4988235
|
LCT
-13910C>T
|
Lactase persistence - ability to digest lactose (milk sugar) in adulthood
|
Methylation & Detox
|
|
Established
|
|
rs61816766
|
FLG
Filaggrin second variant
|
Intronic FLG-locus variant strongly associated with atopic dermatitis — the C...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs7192
|
HLA-DRA
HLA-DRA Leu242Val
|
Missense variant (Leu242Val) in the HLA-DRA alpha chain; the T allele tags HL...
|
Allergy & Atopic Disease
|
|
Strong
|
|
rs9275596
|
HLA-DQ
HLA-DQ Region Peanut Allergy Locus
|
Intergenic tag SNP between HLA-DQB1 and HLA-DQA2 tagging the HLA-DQA1*01:02 r...
|
Allergy & Atopic Disease
|
|
Strong
|