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rs9380516

From SNPedia

Orientationplus
Stabilizedplus
Make rs9380516(C;C)
Make rs9380516(C;T)
Make rs9380516(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position35534425
is asnp
is mentioned by
dbSNPrs9380516
ebirs9380516
HLIrs9380516
Exacrs9380516
Varsomers9380516
Maprs9380516
PheGenIrs9380516
hapmaprs9380516
1000 genomesrs9380516
hgdprs9380516
ensemblrs9380516
gopubmedrs9380516
geneviewrs9380516
scholarrs9380516
googlers9380516
pharmgkbrs9380516
gwascentralrs9380516
openSNPrs9380516
23andMers9380516
23andMe allrs9380516
SNP Nexus

SNPshotrs9380516
SNPdbers9380516
MSV3drs9380516
GWAS Ctlgrs9380516
GMAF0.1433
Max Magnitude
? (C;C) (C;T) (T;T) 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 T
P-val 5E-7
Odds Ratio NR NR