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rs9405098

From SNPedia

Orientationplus
Stabilizedplus
Make rs9405098(A;A)
Make rs9405098(A;G)
Make rs9405098(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position32411959
is asnp
is mentioned by
dbSNPrs9405098
ebirs9405098
HLIrs9405098
Exacrs9405098
Varsomers9405098
Maprs9405098
PheGenIrs9405098
hapmaprs9405098
1000 genomesrs9405098
hgdprs9405098
ensemblrs9405098
gopubmedrs9405098
geneviewrs9405098
scholarrs9405098
googlers9405098
pharmgkbrs9405098
gwascentralrs9405098
openSNPrs9405098
23andMers9405098
23andMe allrs9405098
SNP Nexus

SNPshotrs9405098
SNPdbers9405098
MSV3drs9405098
GWAS Ctlgrs9405098
GMAF0.08356
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23321320]
Trait Hepatitis C induced liver cirrhosis
Title A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region.
Risk Allele A
P-val 1E-10
Odds Ratio 1.37 [1.24-1.51]