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rs16851720

From SNPedia

Orientationplus
Stabilizedplus
Make rs16851720(A;A)
Make rs16851720(A;C)
Make rs16851720(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position141744456
GeneRNF7
is asnp
is mentioned by
dbSNPrs16851720
ebirs16851720
HLIrs16851720
Exacrs16851720
Varsomers16851720
Maprs16851720
PheGenIrs16851720
hapmaprs16851720
1000 genomesrs16851720
hgdprs16851720
ensemblrs16851720
gopubmedrs16851720
geneviewrs16851720
scholarrs16851720
googlers16851720
pharmgkbrs16851720
gwascentralrs16851720
openSNPrs16851720
23andMers16851720
23andMe allrs16851720
SNP Nexus

SNPshotrs16851720
SNPdbers16851720
MSV3drs16851720
GWAS Ctlgrs16851720
GMAF0.1846
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 9E-9
Odds Ratio NR NR