rs149840927
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs149840927(G;T) |
| Make rs149840927(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 14 |
| Position | 23423672 |
| Gene | MYH7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149840927 |
| dbSNP (classic) | rs149840927 |
| ClinGen | rs149840927 |
| ebi | rs149840927 |
| HLI | rs149840927 |
| Exac | rs149840927 |
| Gnomad | rs149840927 |
| Varsome | rs149840927 |
| LitVar | rs149840927 |
| Map | rs149840927 |
| PheGenI | rs149840927 |
| Biobank | rs149840927 |
| 1000 genomes | rs149840927 |
| hgdp | rs149840927 |
| ensembl | rs149840927 |
| geneview | rs149840927 |
| scholar | rs149840927 |
| rs149840927 | |
| pharmgkb | rs149840927 |
| gwascentral | rs149840927 |
| openSNP | rs149840927 |
| 23andMe | rs149840927 |
| SNPshot | rs149840927 |
| SNPdbe | rs149840927 |
| MSV3d | rs149840927 |
| GWAS Ctlg | rs149840927 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs149840927(T;T) |
| Alt | rs149840927(T;T) |
| Reference | Rs149840927(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MYH7 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000014.8:g.23892881G>T |
| CLNSRC | |
| CLNACC | RCV000158581.2, |
