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rs2694917

From SNPedia

Orientationplus
Stabilizedplus
Make rs2694917(C;C)
Make rs2694917(C;T)
Make rs2694917(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position56519080
is asnp
is mentioned by
dbSNPrs2694917
ebirs2694917
HLIrs2694917
Exacrs2694917
Varsomers2694917
Maprs2694917
PheGenIrs2694917
hapmaprs2694917
1000 genomesrs2694917
hgdprs2694917
ensemblrs2694917
gopubmedrs2694917
geneviewrs2694917
scholarrs2694917
googlers2694917
pharmgkbrs2694917
gwascentralrs2694917
openSNPrs2694917
23andMers2694917
23andMe allrs2694917
SNP Nexus

SNPshotrs2694917
SNPdbers2694917
MSV3drs2694917
GWAS Ctlgrs2694917
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24816252OA-icon.png]
Trait Blood metabolite ratios
Title An atlas of genetic influences on human blood metabolites.
Risk Allele T
P-val 2E-29
Odds Ratio .02 [0.014-0.022] unit increase