rs436857
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs436857(A;A) |
| Make rs436857(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 18086825 |
| Gene | IL12RB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs436857 |
| dbSNP (classic) | rs436857 |
| ClinGen | rs436857 |
| ebi | rs436857 |
| HLI | rs436857 |
| Exac | rs436857 |
| Gnomad | rs436857 |
| Varsome | rs436857 |
| LitVar | rs436857 |
| Map | rs436857 |
| PheGenI | rs436857 |
| Biobank | rs436857 |
| 1000 genomes | rs436857 |
| hgdp | rs436857 |
| ensembl | rs436857 |
| geneview | rs436857 |
| scholar | rs436857 |
| rs436857 | |
| pharmgkb | rs436857 |
| gwascentral | rs436857 |
| openSNP | rs436857 |
| 23andMe | rs436857 |
| SNPshot | rs436857 |
| SNPdbe | rs436857 |
| MSV3d | rs436857 |
| GWAS Ctlg | rs436857 |
| GMAF | 0.1433 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 16600026
] Asthma families show transmission disequilibrium of gene variants in the vitamin D metabolism and signalling pathway.
[PMID 19235914] Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease.
[PMID 20525402] Analysis of eight genes modulating interferon gamma and human genetic susceptibility to tuberculosis: a case-control association study.
[PMID 20617178] Leprosy and the adaptation of human toll-like receptor 1.
| ClinVar | |
|---|---|
| Risk | rs436857(A;A) |
| Alt | rs436857(A;A) |
| Reference | Rs436857(G;G) |
| Significance | Non-pathogenic |
| Disease | Familial Atypical Mycobacteriosis not specified |
| Variation | info |
| Gene | IL12RB1 |
| CLNDBN | Familial Atypical Mycobacteriosis, Autosomal Recessive not specified |
| Reversed | 0 |
| HGVS | NC_000019.9:g.18197635G>A |
| CLNSRC | |
| CLNACC | RCV000368982.1, RCV000454669.1, |
