rs1133779
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs1133779(C;C) |
| Make rs1133779(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 44297667 |
| Gene | AIRE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1133779 |
| dbSNP (classic) | rs1133779 |
| ClinGen | rs1133779 |
| ebi | rs1133779 |
| HLI | rs1133779 |
| Exac | rs1133779 |
| Gnomad | rs1133779 |
| Varsome | rs1133779 |
| LitVar | rs1133779 |
| Map | rs1133779 |
| PheGenI | rs1133779 |
| Biobank | rs1133779 |
| 1000 genomes | rs1133779 |
| hgdp | rs1133779 |
| ensembl | rs1133779 |
| geneview | rs1133779 |
| scholar | rs1133779 |
| rs1133779 | |
| pharmgkb | rs1133779 |
| gwascentral | rs1133779 |
| openSNP | rs1133779 |
| 23andMe | rs1133779 |
| SNPshot | rs1133779 |
| SNPdbe | rs1133779 |
| MSV3d | rs1133779 |
| GWAS Ctlg | rs1133779 |
| Merged from | Rs1800522 |
| GMAF | 0.4573 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20363194] The role of AIRE polymorphisms in melanoma.
| ClinVar | |
|---|---|
| Risk | rs1133779(C;C) |
| Alt | rs1133779(C;C) |
| Reference | Rs1133779(T;T) |
| Significance | Other |
| Disease | not specified |
| Variation | info |
| Gene | AIRE |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000021.8:g.45717550T>C |
| CLNSRC | ClinVar University of Chicago |
| CLNACC | RCV000116300.3, |
