rs193922620
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs193922620(A;A) |
| Make rs193922620(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 1 |
| Position | 201359618 |
| Gene | TNNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs193922620 |
| dbSNP (classic) | rs193922620 |
| ClinGen | rs193922620 |
| ebi | rs193922620 |
| HLI | rs193922620 |
| Exac | rs193922620 |
| Gnomad | rs193922620 |
| Varsome | rs193922620 |
| LitVar | rs193922620 |
| Map | rs193922620 |
| PheGenI | rs193922620 |
| Biobank | rs193922620 |
| 1000 genomes | rs193922620 |
| hgdp | rs193922620 |
| ensembl | rs193922620 |
| geneview | rs193922620 |
| scholar | rs193922620 |
| rs193922620 | |
| pharmgkb | rs193922620 |
| gwascentral | rs193922620 |
| openSNP | rs193922620 |
| 23andMe | rs193922620 |
| SNPshot | rs193922620 |
| SNPdbe | rs193922620 |
| MSV3d | rs193922620 |
| GWAS Ctlg | rs193922620 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs193922620(A;A) |
| Alt | rs193922620(A;A) |
| Reference | Rs193922620(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Cardiomyopathy not provided |
| Variation | info |
| Gene | TNNT2 |
| CLNDBN | Cardiomyopathy not provided |
| Reversed | 1 |
| HGVS | NC_000001.10:g.201328746C>T |
| CLNSRC | |
| CLNACC | RCV000030568.1, RCV000225739.1, |
