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rs883924

From SNPedia

Orientationplus
Stabilizedplus
Make rs883924(A;A)
Make rs883924(A;G)
Make rs883924(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position90419249
GeneRP11-389K14.3
is asnp
is mentioned by
dbSNPrs883924
ebirs883924
HLIrs883924
Exacrs883924
Varsomers883924
Maprs883924
PheGenIrs883924
hapmaprs883924
1000 genomesrs883924
hgdprs883924
ensemblrs883924
gopubmedrs883924
geneviewrs883924
scholarrs883924
googlers883924
pharmgkbrs883924
gwascentralrs883924
openSNPrs883924
23andMers883924
23andMe allrs883924
SNP Nexus

SNPshotrs883924
SNPdbers883924
MSV3drs883924
GWAS Ctlgrs883924
GMAF0.3343
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 A
P-val 2E-6
Odds Ratio NR NR