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rs10177833
|
SLC4A5
|
Intronic variant in the sodium bicarbonate cotransporter gene strongly associ...
|
Blood Pressure & Hypertension
|
|
Strong
|
|
rs1165196
|
SLC17A1
SLC17A1 T269I (NPT1)
|
Missense variant in SLC17A1 (NPT1) encoding a Thr269Ile substitution; the G a...
|
Uric Acid & Kidney Function
|
|
Moderate
|
|
rs1165205
|
SLC17A3
SLC17A3 variant (NPT4)
|
Intronic variant in SLC17A3, encoding the renal apical urate efflux transport...
|
Uric Acid & Kidney Function
|
|
Moderate
|
|
rs11950646
|
SLC23A1
|
Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT...
|
Vitamins & Nutrient Absorption
|
|
Moderate
|
|
rs1183201
|
SLC17A1
|
Intronic variant in SLC17A1 (NPT1), the renal apical urate efflux transporter...
|
Uric Acid & Kidney Function
|
|
Strong
|
|
rs12510549
|
SLC2A9
|
Intergenic variant in the SLC2A9 urate-transporter locus — the C allele is as...
|
Uric Acid & Kidney Function
|
|
Strong
|
|
rs147647315
|
SLC22A12
URAT1 R90H
|
Missense variant in URAT1 reducing urate reabsorption in the kidney, causing ...
|
Uric Acid & Kidney Function
|
|
Strong
|
|
rs12704795
|
PON2
PON2 intron 1 variant
|
Intronic PON2 haplotype tag; the A allele is associated with reduced intracel...
|
Vascular Inflammation & Remodeling
|
|
Moderate
|
|
rs35929607
|
STK39
|
Intronic variant in the SPAK kinase gene that has been studied for associatio...
|
Blood Pressure & Hypertension
|
|
Emerging
|
|
rs146582474
|
SLC7A7
|
Finnish founder splice acceptor mutation abolishing y+LAT1 transport activity...
|
Metabolic Enzymes & Rare Disorders
|
|
Established
|
|
rs3755351
|
ADD2
|
Intronic variant in beta-adducin modulating renal Na+/K+-ATPase trafficking a...
|
Blood Pressure & Hypertension
|
|
Emerging
|
|
rs3825016
|
SLC22A12
|
Synonymous coding variant in the URAT1 renal urate transporter; the C allele ...
|
Uric Acid & Kidney Function
|
|
Moderate
|
|
rs3865418
|
NEDD4L
|
Intronic NEDD4L variant that tags reduced ubiquitin-ligase activity toward th...
|
Blood Pressure & Hypertension
|
|
Moderate
|
|
rs7305099
|
WNK1
WNK1 intronic variant
|
Intronic WNK1 variant where the G allele is associated with increased essenti...
|
Blood Pressure & Hypertension
|
|
Moderate
|
|
rs73885316
|
APOL1
p.N264K
|
Protective missense modifier in APOL1 that abolishes G2 risk allele cytotoxic...
|
Uric Acid & Kidney Function
|
|
Strong
|
|
rs193922485
|
HNF1B
|
Rare HNF1B splice-region intronic variant of uncertain significance, found ne...
|
Blood Sugar & Diabetes
|
|
Emerging
|
|
rs73885319
|
APOL1
G1 S342G
|
APOL1 G1 kidney disease risk variant — missense change that evolved for trypa...
|
Cholesterol & Lipoproteins
|
|
Established
|
|
rs6596471
|
SLC23A1
SLC23A1 variant
|
Intronic variant in the intestinal and renal vitamin C transporter gene (SVCT...
|
Vitamins & Nutrient Absorption
|
|
Moderate
|