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rs3776331

From SNPedia

Orientationminus
Stabilizedminus
Make rs3776331(A;A)
Make rs3776331(A;G)
Make rs3776331(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position143062229
GeneARHGAP26
is asnp
is mentioned by
dbSNPrs3776331
ebirs3776331
HLIrs3776331
Exacrs3776331
Varsomers3776331
Maprs3776331
PheGenIrs3776331
hapmaprs3776331
1000 genomesrs3776331
hgdprs3776331
ensemblrs3776331
gopubmedrs3776331
geneviewrs3776331
scholarrs3776331
googlers3776331
pharmgkbrs3776331
gwascentralrs3776331
openSNPrs3776331
23andMers3776331
23andMe allrs3776331
SNP Nexus

SNPshotrs3776331
SNPdbers3776331
MSV3drs3776331
GWAS Ctlgrs3776331
GMAF0.2681
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18759275OA-icon.png]
Trait Serum uric acid
Title Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish
Risk Allele
P-val 0.0000079999999999999996
Odds Ratio 0.30 [NR] mg/dl increase in uric acid levels


GET Evidence
rs3776331
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.742188
summary