[PMID 20714752] IFNG +874 T>A single nucleotide polymorphism is associated with leprosy among Brazilians

[PMID 21067287] Multiple sclerosis risk markers in HLA-DRA, HLA-C, and IFNG genes are associated with sex-specific childhood leukemia risk


[PMID 20587610] Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection

[PMID 15726497] Gene-environment interaction effects on the development of immune responses in the 1st year of life.

[PMID 16617143] Algorithm for automatic genotype calling of single nucleotide polymorphisms using the full course of TaqMan real-time data.

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

[PMID 18332247] Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expression.

[PMID 18365030] Host genetic factors and vaccine-induced immunity to hepatitis B virus infection.

[PMID 18385742] A single nucleotide polymorphism (A --> G) in intron 3 of IFNgamma gene is associated with asthma.

[PMID 20806065] Host genetic factors and vaccine-induced immunity to HBV infection: haplotype analysis.

[PMID 21798578] IFNG genotype and sex interact to influence the risk of childhood asthma.


[PMID 25445652] Interferon-γ (IFNG) microsatellite repeat and single nucleotide polymorphism haplotypes of IFN-α receptor (IFNAR1) associated with enhanced malaria susceptibility in Indian populations

rs2069727

Parent Gene: IFNG

Importance: 1
Less common allele: C = 28%
More common allele: T = 72%
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