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rs2629751

From SNPedia

Orientationplus
Stabilizedplus
Make rs2629751(A;A)
Make rs2629751(A;G)
Make rs2629751(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position104028030
GeneGLT8D2
is asnp
is mentioned by
dbSNPrs2629751
ebirs2629751
HLIrs2629751
Exacrs2629751
Varsomers2629751
Maprs2629751
PheGenIrs2629751
hapmaprs2629751
1000 genomesrs2629751
hgdprs2629751
ensemblrs2629751
gopubmedrs2629751
geneviewrs2629751
scholarrs2629751
googlers2629751
pharmgkbrs2629751
gwascentralrs2629751
openSNPrs2629751
23andMers2629751
23andMe allrs2629751
SNP Nexus

SNPshotrs2629751
SNPdbers2629751
MSV3drs2629751
GWAS Ctlgrs2629751
GMAF0.3421
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22841784OA-icon.png]
Trait Hepatitis C induced liver fibrosis
Title Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.
Risk Allele G
P-val 1E-7
Odds Ratio NR NR