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rs1106766

From SNPedia

Orientationplus
Stabilizedplus
Make rs1106766(C;C)
Make rs1106766(C;T)
Make rs1106766(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position57415673
GeneR3HDM2
is asnp
is mentioned by
dbSNPrs1106766
ebirs1106766
HLIrs1106766
Exacrs1106766
Varsomers1106766
Maprs1106766
PheGenIrs1106766
hapmaprs1106766
1000 genomesrs1106766
hgdprs1106766
ensemblrs1106766
gopubmedrs1106766
geneviewrs1106766
scholarrs1106766
googlers1106766
pharmgkbrs1106766
gwascentralrs1106766
openSNPrs1106766
23andMers1106766
23andMe allrs1106766
SNP Nexus

SNPshotrs1106766
SNPdbers1106766
MSV3drs1106766
GWAS Ctlgrs1106766
GMAF0.1547
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20884846OA-icon.png]
Trait
Title Multiple Genetic Loci Influence Serum Urate And Their Relationship With Gout and Cardiovascular Disease Risk Factors
Risk Allele T
P-val 2E-11
Odds Ratio 5.16 [3.65-6.67] umol/l decrease


[PMID 26427508] Serum urate gene associations with incident gout, measured in the Framingham Heart Study, are modified by renal disease and not by body mass index