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rs12137855

From SNPedia

Orientationplus
Stabilizedplus
Make rs12137855(C;C)
Make rs12137855(C;T)
Make rs12137855(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position219275036
is asnp
is mentioned by
dbSNPrs12137855
ebirs12137855
HLIrs12137855
Exacrs12137855
Varsomers12137855
Maprs12137855
PheGenIrs12137855
hapmaprs12137855
1000 genomesrs12137855
hgdprs12137855
ensemblrs12137855
gopubmedrs12137855
geneviewrs12137855
scholarrs12137855
googlers12137855
pharmgkbrs12137855
gwascentralrs12137855
openSNPrs12137855
23andMers12137855
23andMe allrs12137855
SNP Nexus

SNPshotrs12137855
SNPdbers12137855
MSV3drs12137855
GWAS Ctlgrs12137855
GMAF0.1648
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24477042] Genetic variants in GCKR and PNPLA3 confer susceptibility to nonalcoholic fatty liver disease in obese individuals


[PMID 21423719OA-icon.png] Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.