rs28934269
From SNPedia
| Merged into | rs104894502 |
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | |
| (A;G) | 3 | Familial Hypertrophic Cardiomyopathy |
| (G;G) | 3 | Familial Hypertrophic Cardiomyopathy |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 63060915 |
| Gene | TPM1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28934269 |
| dbSNP (classic) | rs28934269 |
| ClinGen | rs28934269 |
| ebi | rs28934269 |
| HLI | rs28934269 |
| Exac | rs28934269 |
| Gnomad | rs28934269 |
| Varsome | rs28934269 |
| LitVar | rs28934269 |
| Map | rs28934269 |
| PheGenI | rs28934269 |
| Biobank | rs28934269 |
| 1000 genomes | rs28934269 |
| hgdp | rs28934269 |
| ensembl | rs28934269 |
| geneview | rs28934269 |
| scholar | rs28934269 |
| rs28934269 | |
| pharmgkb | rs28934269 |
| gwascentral | rs28934269 |
| openSNP | rs28934269 |
| 23andMe | rs28934269 |
| SNPshot | rs28934269 |
| SNPdbe | rs28934269 |
| MSV3d | rs28934269 |
| GWAS Ctlg | rs28934269 |
| Status | Merged into rs104894502 |
| Max Magnitude | 3 |
Familial hypertrophic cardiomyopathy
see also OMIM 191010.0001
Note: This SNP, rs28934269, appears to identify the exact same polymorphic location as rs104894502.
