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rs2069707

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2069707(C;G)
Make rs2069707(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position68160508
GeneIFNG
is asnp
is mentioned by
dbSNPrs2069707
ebirs2069707
HLIrs2069707
Exacrs2069707
Varsomers2069707
Maprs2069707
PheGenIrs2069707
hapmaprs2069707
1000 genomesrs2069707
hgdprs2069707
ensemblrs2069707
gopubmedrs2069707
geneviewrs2069707
scholarrs2069707
googlers2069707
pharmgkbrs2069707
gwascentralrs2069707
openSNPrs2069707
23andMers2069707
23andMe allrs2069707
SNP Nexus

SNPshotrs2069707
SNPdbers2069707
MSV3drs2069707
GWAS Ctlgrs2069707
GMAF0.02617
Max Magnitude0
? (C;C) (C;G) (G;G) 28
OMIM609532
DescHEPATITIS C VIRUS, SUSCEPTIBILITY TO
Variant
Relatedalso
OMIM147570
DescINTERFERON, GAMMA; IFNG
Variant
Relatedalso
OMIM147570
Desc
Variant0004
Relatedalso
[PMID 17215375OA-icon.png] A functional SNP of interferon-gamma gene is important for interferon-alpha-induced and spontaneous recovery from hepatitis C virus infection.


[PMID 19126646OA-icon.png] Genetic polymorphisms in the cytokine genes and risk of hepatocellular carcinoma in low-risk non-Asians of USA.


[PMID 25798684] Role of Interferon Gamma and Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand Receptor 1 Single Nucleotide Polymorphism in Natural Clearance and Treatment Response of HCV Infection