rs201564919
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs201564919(A;A) |
| Make rs201564919(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 18 |
| Position | 31541225 |
| Gene | DSG2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201564919 |
| dbSNP (classic) | rs201564919 |
| ClinGen | rs201564919 |
| ebi | rs201564919 |
| HLI | rs201564919 |
| Exac | rs201564919 |
| Gnomad | rs201564919 |
| Varsome | rs201564919 |
| LitVar | rs201564919 |
| Map | rs201564919 |
| PheGenI | rs201564919 |
| Biobank | rs201564919 |
| 1000 genomes | rs201564919 |
| hgdp | rs201564919 |
| ensembl | rs201564919 |
| geneview | rs201564919 |
| scholar | rs201564919 |
| rs201564919 | |
| pharmgkb | rs201564919 |
| gwascentral | rs201564919 |
| openSNP | rs201564919 |
| 23andMe | rs201564919 |
| SNPshot | rs201564919 |
| SNPdbe | rs201564919 |
| MSV3d | rs201564919 |
| GWAS Ctlg | rs201564919 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201564919(A;A) |
| Alt | rs201564919(A;A) |
| Reference | Rs201564919(G;G) |
| Significance | Pathogenic |
| Disease | Arrhythmogenic right ventricular cardiomyopathy not specified |
| Variation | info |
| Gene | DSG2 |
| CLNDBN | Arrhythmogenic right ventricular cardiomyopathy not specified |
| Reversed | 0 |
| HGVS | NC_000018.9:g.29121188G>A |
| CLNSRC | |
| CLNACC | RCV000148474.1, RCV000154703.1, |
