rs144120198
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs144120198(A;A) |
| Make rs144120198(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32443193 |
| Gene | HLA-DRA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs144120198 |
| dbSNP (classic) | rs144120198 |
| ClinGen | rs144120198 |
| ebi | rs144120198 |
| HLI | rs144120198 |
| Exac | rs144120198 |
| Gnomad | rs144120198 |
| Varsome | rs144120198 |
| LitVar | rs144120198 |
| Map | rs144120198 |
| PheGenI | rs144120198 |
| Biobank | rs144120198 |
| 1000 genomes | rs144120198 |
| hgdp | rs144120198 |
| ensembl | rs144120198 |
| geneview | rs144120198 |
| scholar | rs144120198 |
| rs144120198 | |
| pharmgkb | rs144120198 |
| gwascentral | rs144120198 |
| openSNP | rs144120198 |
| 23andMe | rs144120198 |
| SNPshot | rs144120198 |
| SNPdbe | rs144120198 |
| MSV3d | rs144120198 |
| GWAS Ctlg | rs144120198 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs144120198(A;A) |
| Alt | rs144120198(A;A) |
| Reference | Rs144120198(G;G) |
| Significance | Untested |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | HLA-DRA |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000006.12:g.32443193G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000061399.2, |
[PMID 21499247
] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
