rs797045097
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs797045097(A;A) |
| Make rs797045097(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 14 |
| Position | 23418348 |
| Gene | MIR208B, MYH7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs797045097 |
| dbSNP (classic) | rs797045097 |
| ClinGen | rs797045097 |
| ebi | rs797045097 |
| HLI | rs797045097 |
| Exac | rs797045097 |
| Gnomad | rs797045097 |
| Varsome | rs797045097 |
| LitVar | rs797045097 |
| Map | rs797045097 |
| PheGenI | rs797045097 |
| Biobank | rs797045097 |
| 1000 genomes | rs797045097 |
| hgdp | rs797045097 |
| ensembl | rs797045097 |
| geneview | rs797045097 |
| scholar | rs797045097 |
| rs797045097 | |
| pharmgkb | rs797045097 |
| gwascentral | rs797045097 |
| openSNP | rs797045097 |
| 23andMe | rs797045097 |
| SNPshot | rs797045097 |
| SNPdbe | rs797045097 |
| MSV3d | rs797045097 |
| GWAS Ctlg | rs797045097 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs797045097(A;A) |
| Alt | rs797045097(A;A) |
| Reference | Rs797045097(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Familial hypertrophic cardiomyopathy 1 not specified not provided |
| Variation | info |
| Gene | MYH7 MIR208B |
| CLNDBN | Familial hypertrophic cardiomyopathy 1 not specified not provided |
| Reversed | 1 |
| HGVS | NC_000014.8:g.23887557C>T |
| CLNSRC | |
| CLNACC | RCV000190606.2, RCV000211873.1, RCV000223729.1, |
