rs1055311
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1055311(C;T) |
| Make rs1055311(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 44289685 |
| Gene | AIRE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1055311 |
| dbSNP (classic) | rs1055311 |
| ClinGen | rs1055311 |
| ebi | rs1055311 |
| HLI | rs1055311 |
| Exac | rs1055311 |
| Gnomad | rs1055311 |
| Varsome | rs1055311 |
| LitVar | rs1055311 |
| Map | rs1055311 |
| PheGenI | rs1055311 |
| Biobank | rs1055311 |
| 1000 genomes | rs1055311 |
| hgdp | rs1055311 |
| ensembl | rs1055311 |
| geneview | rs1055311 |
| scholar | rs1055311 |
| rs1055311 | |
| pharmgkb | rs1055311 |
| gwascentral | rs1055311 |
| openSNP | rs1055311 |
| 23andMe | rs1055311 |
| SNPshot | rs1055311 |
| SNPdbe | rs1055311 |
| MSV3d | rs1055311 |
| GWAS Ctlg | rs1055311 |
| GMAF | 0.1368 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20363194] The role of AIRE polymorphisms in melanoma
| ClinVar | |
|---|---|
| Risk | rs1055311(G;G) rs1055311(T;T) |
| Alt | rs1055311(G;G) rs1055311(T;T) |
| Reference | Rs1055311(C;C) |
| Significance | Other |
| Disease | not specified |
| Variation | info |
| Gene | AIRE |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000021.8:g.45709568C>T |
| CLNSRC | ClinVar University of Chicago |
| CLNACC | RCV000116302.3, |
