rs121913388
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs121913388(C;C) |
| Make rs121913388(C;T) |
| Make rs121913388(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 9 |
| Position | 21971121 |
| Gene | CDKN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121913388 |
| dbSNP (classic) | rs121913388 |
| ClinGen | rs121913388 |
| ebi | rs121913388 |
| HLI | rs121913388 |
| Exac | rs121913388 |
| Gnomad | rs121913388 |
| Varsome | rs121913388 |
| LitVar | rs121913388 |
| Map | rs121913388 |
| PheGenI | rs121913388 |
| Biobank | rs121913388 |
| 1000 genomes | rs121913388 |
| hgdp | rs121913388 |
| ensembl | rs121913388 |
| geneview | rs121913388 |
| scholar | rs121913388 |
| rs121913388 | |
| pharmgkb | rs121913388 |
| gwascentral | rs121913388 |
| openSNP | rs121913388 |
| 23andMe | rs121913388 |
| SNPshot | rs121913388 |
| SNPdbe | rs121913388 |
| MSV3d | rs121913388 |
| GWAS Ctlg | rs121913388 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121913388(G;G) rs121913388(T;T) |
| Alt | rs121913388(G;G) rs121913388(T;T) |
| Reference | rs121913388(C;C) |
| Significance | Other |
| Disease | Melanoma Malignant melanoma |
| Variation | info |
| Gene | CDKN2A |
| CLNDBN | Melanoma, cutaneous malignant, susceptibility to, 2 Malignant melanoma |
| Reversed | 1 |
| HGVS | NC_000009.11:g.21971120G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000010012.2, RCV000429694.1, |
[PMID 21499247
] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.
