rs45476696
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs45476696(A;A) |
| Make rs45476696(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 9 |
| Position | 21970902 |
| Gene | CDKN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs45476696 |
| dbSNP (classic) | rs45476696 |
| ClinGen | rs45476696 |
| ebi | rs45476696 |
| HLI | rs45476696 |
| Exac | rs45476696 |
| Gnomad | rs45476696 |
| Varsome | rs45476696 |
| LitVar | rs45476696 |
| Map | rs45476696 |
| PheGenI | rs45476696 |
| Biobank | rs45476696 |
| 1000 genomes | rs45476696 |
| hgdp | rs45476696 |
| ensembl | rs45476696 |
| geneview | rs45476696 |
| scholar | rs45476696 |
| rs45476696 | |
| pharmgkb | rs45476696 |
| gwascentral | rs45476696 |
| openSNP | rs45476696 |
| 23andMe | rs45476696 |
| SNPshot | rs45476696 |
| SNPdbe | rs45476696 |
| MSV3d | rs45476696 |
| GWAS Ctlg | rs45476696 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs45476696(A;A) rs45476696(T;T) |
| Alt | rs45476696(A;A) rs45476696(T;T) |
| Reference | Rs45476696(G;G) |
| Significance | Pathogenic |
| Disease | Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | CDKN2A |
| CLNDBN | Hereditary cutaneous melanoma Hereditary cancer-predisposing syndrome |
| Reversed | 1 |
| HGVS | NC_000009.11:g.21970901C>A |
| CLNSRC | |
| CLNACC | RCV000198192.3, RCV000223581.2, |
