rs150414818
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | |
(G;G) | 3.5 | increased risk of gout |
Make rs150414818(C;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 49465749 |
Gene | ALDH16A1 |
is a | snp |
is | mentioned by |
dbSNP | rs150414818 |
dbSNP (classic) | rs150414818 |
ClinGen | rs150414818 |
ebi | rs150414818 |
HLI | rs150414818 |
Exac | rs150414818 |
Gnomad | rs150414818 |
Varsome | rs150414818 |
LitVar | rs150414818 |
Map | rs150414818 |
PheGenI | rs150414818 |
Biobank | rs150414818 |
1000 genomes | rs150414818 |
hgdp | rs150414818 |
ensembl | rs150414818 |
geneview | rs150414818 |
scholar | rs150414818 |
rs150414818 | |
pharmgkb | rs150414818 |
gwascentral | rs150414818 |
openSNP | rs150414818 |
23andMe | rs150414818 |
SNPshot | rs150414818 |
SNPdbe | rs150414818 |
MSV3d | rs150414818 |
GWAS Ctlg | rs150414818 |
Max Magnitude | 3.5 |
a low-frequency missense variant rs150414818 (c.1580C>G) in ALDH16A1 associated with gout (OR = 3.12, P = 1.5 × 10?16, at-risk allele frequency = 0.019) and serum uric acid levels (effect = 0.36 s.d., P = 4.5 × 10?21) nature genetics