rs2069707

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs2069707(C;G)

Make rs2069707(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

68160508

Gene

IFNG

is a	snp
is	mentioned by
dbSNP	rs2069707
dbSNP (classic)	rs2069707
ClinGen	rs2069707
ebi	rs2069707
HLI	rs2069707
Exac	rs2069707
Gnomad	rs2069707
Varsome	rs2069707
LitVar	rs2069707
Map	rs2069707
PheGenI	rs2069707
Biobank	rs2069707
1000 genomes	rs2069707
hgdp	rs2069707
ensembl	rs2069707
geneview	rs2069707
scholar	rs2069707
google	rs2069707
pharmgkb	rs2069707
gwascentral	rs2069707
openSNP	rs2069707
23andMe	rs2069707
SNPshot	rs2069707
SNPdbe	rs2069707
MSV3d	rs2069707
GWAS Ctlg	rs2069707

GMAF

0.02617

Max Magnitude

0

?

(C;C) (C;G) (G;G)

28

OMIM	609532
Desc	HEPATITIS C VIRUS, SUSCEPTIBILITY TO
Variant
Related	also

OMIM	147570
Desc	INTERFERON, GAMMA; IFNG
Variant
Related	also

OMIM	147570
Desc
Variant	0004
Related	also

[PMID 17215375 ] A functional SNP of interferon-gamma gene is important for interferon-alpha-induced and spontaneous recovery from hepatitis C virus infection.

[PMID 19126646 ] 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

ClinVar
Risk	rs2069707(G;G)
Alt	rs2069707(G;G)
Reference	Rs2069707(C;C)
Significance	Drug-response
Disease	Hepatitis C virus infection
Variation	info
Gene	IFNG
CLNDBN	Hepatitis C virus infection, response to therapy of
Reversed	1
HGVS	NC_000012.11:g.68554288G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015846.3,