rs2069727
| Orientation | minus |
| Stabilized | minus |
| Make rs2069727(A;A) |
| Make rs2069727(A;G) |
| Make rs2069727(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 68154443 |
| Gene | IFNG |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2069727 |
| dbSNP (classic) | rs2069727 |
| ClinGen | rs2069727 |
| ebi | rs2069727 |
| HLI | rs2069727 |
| Exac | rs2069727 |
| Gnomad | rs2069727 |
| Varsome | rs2069727 |
| LitVar | rs2069727 |
| Map | rs2069727 |
| PheGenI | rs2069727 |
| Biobank | rs2069727 |
| 1000 genomes | rs2069727 |
| hgdp | rs2069727 |
| ensembl | rs2069727 |
| geneview | rs2069727 |
| scholar | rs2069727 |
| rs2069727 | |
| pharmgkb | rs2069727 |
| gwascentral | rs2069727 |
| openSNP | rs2069727 |
| 23andMe | rs2069727 |
| SNPshot | rs2069727 |
| SNPdbe | rs2069727 |
| MSV3d | rs2069727 |
| GWAS Ctlg | rs2069727 |
| GMAF | 0.2704 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[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
[PMID 26893439] Interaction Between Polymorphisms of IFN-γ and MICA Correlated with Hepatocellular Carcinoma.
