rs9405098

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs9405098(A;A)

Make rs9405098(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

32411959

is a	snp
is	mentioned by
dbSNP	rs9405098
dbSNP (classic)	rs9405098
ClinGen	rs9405098
ebi	rs9405098
HLI	rs9405098
Exac	rs9405098
Gnomad	rs9405098
Varsome	rs9405098
LitVar	rs9405098
Map	rs9405098
PheGenI	rs9405098
Biobank	rs9405098
1000 genomes	rs9405098
hgdp	rs9405098
ensembl	rs9405098
geneview	rs9405098
scholar	rs9405098
google	rs9405098
pharmgkb	rs9405098
gwascentral	rs9405098
openSNP	rs9405098
23andMe	rs9405098
SNPshot	rs9405098
SNPdbe	rs9405098
MSV3d	rs9405098
GWAS Ctlg	rs9405098

GMAF

0.08356

Max Magnitude

0

?	(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]