rs36204594
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;C) | 7 | Pancreatic cancer/Melanoma Syndrome |
| (C;C) | 0 | common in clinvar |
| Make rs36204594(C;T) |
| Make rs36204594(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 9 |
| Position | 21971180 |
| Gene | CDKN2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs36204594 |
| dbSNP (classic) | rs36204594 |
| ClinGen | rs36204594 |
| ebi | rs36204594 |
| HLI | rs36204594 |
| Exac | rs36204594 |
| Gnomad | rs36204594 |
| Varsome | rs36204594 |
| LitVar | rs36204594 |
| Map | rs36204594 |
| PheGenI | rs36204594 |
| Biobank | rs36204594 |
| 1000 genomes | rs36204594 |
| hgdp | rs36204594 |
| ensembl | rs36204594 |
| geneview | rs36204594 |
| scholar | rs36204594 |
| rs36204594 | |
| pharmgkb | rs36204594 |
| gwascentral | rs36204594 |
| openSNP | rs36204594 |
| 23andMe | rs36204594 |
| SNPshot | rs36204594 |
| SNPdbe | rs36204594 |
| MSV3d | rs36204594 |
| GWAS Ctlg | rs36204594 |
| Max Magnitude | 7 |
| ClinVar | |
|---|---|
| Risk | rs36204594(A;A) |
| Alt | rs36204594(A;A) |
| Reference | Rs36204594(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Hereditary cancer-predisposing syndrome |
| Variation | info |
| Gene | CDKN2A |
| CLNDBN | Hereditary cancer-predisposing syndrome |
| Reversed | 1 |
| HGVS | NC_000009.11:g.21971179G>T |
| CLNSRC | |
| CLNACC | RCV000165798.1, |
