rs559848002
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs559848002(C;C) |
| Make rs559848002(C;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 9 |
| Position | 21971147 |
| Gene | CDKN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs559848002 |
| dbSNP (classic) | rs559848002 |
| ClinGen | rs559848002 |
| ebi | rs559848002 |
| HLI | rs559848002 |
| Exac | rs559848002 |
| Gnomad | rs559848002 |
| Varsome | rs559848002 |
| LitVar | rs559848002 |
| Map | rs559848002 |
| PheGenI | rs559848002 |
| Biobank | rs559848002 |
| 1000 genomes | rs559848002 |
| hgdp | rs559848002 |
| ensembl | rs559848002 |
| geneview | rs559848002 |
| scholar | rs559848002 |
| rs559848002 | |
| pharmgkb | rs559848002 |
| gwascentral | rs559848002 |
| openSNP | rs559848002 |
| 23andMe | rs559848002 |
| SNPshot | rs559848002 |
| SNPdbe | rs559848002 |
| MSV3d | rs559848002 |
| GWAS Ctlg | rs559848002 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs559848002(C;C) rs559848002(G;G) |
| Alt | rs559848002(C;C) rs559848002(G;G) |
| Reference | Rs559848002(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | CDKN2A |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000009.11:g.21971146T>C |
| CLNSRC | |
| CLNACC | RCV000478806.1, |
