rs11914
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs11914(G;G) |
| Make rs11914(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 137198451 |
| Gene | IFNGR1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11914 |
| dbSNP (classic) | rs11914 |
| ClinGen | rs11914 |
| ebi | rs11914 |
| HLI | rs11914 |
| Exac | rs11914 |
| Gnomad | rs11914 |
| Varsome | rs11914 |
| LitVar | rs11914 |
| Map | rs11914 |
| PheGenI | rs11914 |
| Biobank | rs11914 |
| 1000 genomes | rs11914 |
| hgdp | rs11914 |
| ensembl | rs11914 |
| geneview | rs11914 |
| scholar | rs11914 |
| rs11914 | |
| pharmgkb | rs11914 |
| gwascentral | rs11914 |
| openSNP | rs11914 |
| 23andMe | rs11914 |
| SNPshot | rs11914 |
| SNPdbe | rs11914 |
| MSV3d | rs11914 |
| GWAS Ctlg | rs11914 |
| GMAF | 0.1093 |
| Max Magnitude | 0 |
[PMID 20412699] Lack of association between IFNGR1 gene polymorphisms and biopsy-proven giant cell arteritis
[PMID 19356949
] Cytokine SNPs: Comparison of allele frequencies by race and implications for future studies.
| ClinVar | |
|---|---|
| Risk | rs11914(C;C) rs11914(G;G) |
| Alt | rs11914(C;C) rs11914(G;G) |
| Reference | Rs11914(T;T) |
| Significance | Probable-non-pathogenic |
| Disease | Familial Atypical Mycobacteriosis not specified |
| Variation | info |
| Gene | IFNGR1 |
| CLNDBN | Familial Atypical Mycobacteriosis, Autosomal Recessive not specified |
| Reversed | 1 |
| HGVS | NC_000006.11:g.137519588A>C |
| CLNSRC | |
| CLNACC | RCV000313682.1, RCV000455568.1, |
