rs112179534
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs112179534(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 47341246 |
| Gene | MYBPC3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112179534 |
| dbSNP (classic) | rs112179534 |
| ClinGen | rs112179534 |
| ebi | rs112179534 |
| HLI | rs112179534 |
| Exac | rs112179534 |
| Gnomad | rs112179534 |
| Varsome | rs112179534 |
| LitVar | rs112179534 |
| Map | rs112179534 |
| PheGenI | rs112179534 |
| Biobank | rs112179534 |
| 1000 genomes | rs112179534 |
| hgdp | rs112179534 |
| ensembl | rs112179534 |
| geneview | rs112179534 |
| scholar | rs112179534 |
| rs112179534 | |
| pharmgkb | rs112179534 |
| gwascentral | rs112179534 |
| openSNP | rs112179534 |
| 23andMe | rs112179534 |
| SNPshot | rs112179534 |
| SNPdbe | rs112179534 |
| MSV3d | rs112179534 |
| GWAS Ctlg | rs112179534 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs112179534(G;G) |
| Alt | rs112179534(G;G) |
| Reference | Rs112179534(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | MYBPC3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.47362797T>G |
| CLNSRC | |
| CLNACC | RCV000158116.1, |
