Have questions? Visit https://www.reddit.com/r/SNPedia

rs150414818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
(G;G) 3.5 increased risk of gout
Make rs150414818(C;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position49465749
GeneALDH16A1
is asnp
is mentioned by
dbSNPrs150414818
ebirs150414818
HLIrs150414818
Exacrs150414818
Varsomers150414818
Maprs150414818
PheGenIrs150414818
hapmaprs150414818
1000 genomesrs150414818
hgdprs150414818
ensemblrs150414818
gopubmedrs150414818
geneviewrs150414818
scholarrs150414818
googlers150414818
pharmgkbrs150414818
gwascentralrs150414818
openSNPrs150414818
23andMers150414818
23andMe allrs150414818
SNP Nexus

SNPshotrs150414818
SNPdbers150414818
MSV3drs150414818
GWAS Ctlgrs150414818
Max Magnitude3.5
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