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rs6487679

From SNPedia

Orientationplus
Stabilizedplus
Make rs6487679(C;C)
Make rs6487679(C;T)
Make rs6487679(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position9218736
is asnp
is mentioned by
dbSNPrs6487679
ebirs6487679
HLIrs6487679
Exacrs6487679
Varsomers6487679
Maprs6487679
PheGenIrs6487679
hapmaprs6487679
1000 genomesrs6487679
hgdprs6487679
ensemblrs6487679
gopubmedrs6487679
geneviewrs6487679
scholarrs6487679
googlers6487679
pharmgkbrs6487679
gwascentralrs6487679
openSNPrs6487679
23andMers6487679
23andMe allrs6487679
SNP Nexus

SNPshotrs6487679
SNPdbers6487679
MSV3drs6487679
GWAS Ctlgrs6487679
GMAF0.1814
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20708005OA-icon.png]
Trait
Title Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
Risk Allele G
P-val 0.000001
Odds Ratio 0.40 [NR] unit increase