rs141132227
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs141132227(C;T) |
| Make rs141132227(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32814359 |
| Gene | HLA-DOB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141132227 |
| dbSNP (classic) | rs141132227 |
| ClinGen | rs141132227 |
| ebi | rs141132227 |
| HLI | rs141132227 |
| Exac | rs141132227 |
| Gnomad | rs141132227 |
| Varsome | rs141132227 |
| LitVar | rs141132227 |
| Map | rs141132227 |
| PheGenI | rs141132227 |
| Biobank | rs141132227 |
| 1000 genomes | rs141132227 |
| hgdp | rs141132227 |
| ensembl | rs141132227 |
| geneview | rs141132227 |
| scholar | rs141132227 |
| rs141132227 | |
| pharmgkb | rs141132227 |
| gwascentral | rs141132227 |
| openSNP | rs141132227 |
| 23andMe | rs141132227 |
| SNPshot | rs141132227 |
| SNPdbe | rs141132227 |
| MSV3d | rs141132227 |
| GWAS Ctlg | rs141132227 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs141132227(T;T) |
| Alt | rs141132227(T;T) |
| Reference | Rs141132227(C;C) |
| Significance | Untested |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | HLA-DOB |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000006.12:g.32814359C>T |
| CLNSRC | ClinVar |
| CLNACC | RCV000061401.2, |
[PMID 21499247
] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
