rs1085307959
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Chromosome | 14 |
| Position | 23429783 |
| Gene | MYH7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1085307959 |
| dbSNP (classic) | rs1085307959 |
| ClinGen | rs1085307959 |
| ebi | rs1085307959 |
| HLI | rs1085307959 |
| Exac | rs1085307959 |
| Gnomad | rs1085307959 |
| Varsome | rs1085307959 |
| LitVar | rs1085307959 |
| Map | rs1085307959 |
| PheGenI | rs1085307959 |
| Biobank | rs1085307959 |
| 1000 genomes | rs1085307959 |
| hgdp | rs1085307959 |
| ensembl | rs1085307959 |
| geneview | rs1085307959 |
| scholar | rs1085307959 |
| rs1085307959 | |
| pharmgkb | rs1085307959 |
| gwascentral | rs1085307959 |
| openSNP | rs1085307959 |
| 23andMe | rs1085307959 |
| SNPshot | rs1085307959 |
| SNPdbe | rs1085307959 |
| MSV3d | rs1085307959 |
| GWAS Ctlg | rs1085307959 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs1085307959(A;A) |
| Alt | rs1085307959(A;A) |
| Reference | Rs1085307959(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MYH7 |
| CLNDBN | not provided |
| Reversed | 1 |
| HGVS | NC_000014.8:g.23898992C>T |
| CLNSRC | |
| CLNACC | RCV000490207.1, |
