rs535202189
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs535202189(C;T) |
| Make rs535202189(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 211673256 |
| Gene | ERBB4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs535202189 |
| dbSNP (classic) | rs535202189 |
| ClinGen | rs535202189 |
| ebi | rs535202189 |
| HLI | rs535202189 |
| Exac | rs535202189 |
| Gnomad | rs535202189 |
| Varsome | rs535202189 |
| LitVar | rs535202189 |
| Map | rs535202189 |
| PheGenI | rs535202189 |
| Biobank | rs535202189 |
| 1000 genomes | rs535202189 |
| hgdp | rs535202189 |
| ensembl | rs535202189 |
| geneview | rs535202189 |
| scholar | rs535202189 |
| rs535202189 | |
| pharmgkb | rs535202189 |
| gwascentral | rs535202189 |
| openSNP | rs535202189 |
| 23andMe | rs535202189 |
| SNPshot | rs535202189 |
| SNPdbe | rs535202189 |
| MSV3d | rs535202189 |
| GWAS Ctlg | rs535202189 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs535202189(T;T) |
| Alt | rs535202189(T;T) |
| Reference | Rs535202189(C;C) |
| Significance | Probable-Pathogenic |
| Disease | Malignant melanoma |
| Variation | info |
| Gene | ERBB4 |
| CLNDBN | Malignant melanoma |
| Reversed | 0 |
| HGVS | NC_000002.11:g.212537981C>T |
| CLNSRC | |
| CLNACC | RCV000431732.1, |
