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rs2244967

From SNPedia

Orientationplus
Stabilizedplus
Make rs2244967(C;C)
Make rs2244967(C;T)
Make rs2244967(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position49016721
GeneVSTM4
is asnp
is mentioned by
dbSNPrs2244967
ebirs2244967
HLIrs2244967
Exacrs2244967
Varsomers2244967
Maprs2244967
PheGenIrs2244967
hapmaprs2244967
1000 genomesrs2244967
hgdprs2244967
ensemblrs2244967
gopubmedrs2244967
geneviewrs2244967
scholarrs2244967
googlers2244967
pharmgkbrs2244967
gwascentralrs2244967
openSNPrs2244967
23andMers2244967
23andMe allrs2244967
SNP Nexus

SNPshotrs2244967
SNPdbers2244967
MSV3drs2244967
GWAS Ctlgrs2244967
GMAF0.332
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21294900OA-icon.png]
Trait
Title A genome-wide association study of serum uric acid in African Americans
Risk Allele T
P-val 0.000005
Odds Ratio 0.1260 [0.08-0.18] unit decrease