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rs6942328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6942328(C;C)
Make rs6942328(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position4512745
is asnp
is mentioned by
dbSNPrs6942328
ebirs6942328
HLIrs6942328
Exacrs6942328
Varsomers6942328
Maprs6942328
PheGenIrs6942328
hapmaprs6942328
1000 genomesrs6942328
hgdprs6942328
ensemblrs6942328
gopubmedrs6942328
geneviewrs6942328
scholarrs6942328
googlers6942328
pharmgkbrs6942328
gwascentralrs6942328
openSNPrs6942328
23andMers6942328
23andMe allrs6942328
SNP Nexus

SNPshotrs6942328
SNPdbers6942328
MSV3drs6942328
GWAS Ctlgrs6942328
GMAF0.003214
Max Magnitude0
? (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 C
P-val 0.000001
Odds Ratio 0.5450 [0.33-0.77] unit increase