rs779490893
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs779490893(-;-) |
| Make rs779490893(-;CT) |
| Make rs779490893(CT;CT) |
| Reference | GRCh38.p7 38.3/151 |
| Chromosome | 3 |
| Position | 52396983 |
| Gene | DNAH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs779490893 |
| dbSNP (classic) | rs779490893 |
| ClinGen | rs779490893 |
| ebi | rs779490893 |
| HLI | rs779490893 |
| Exac | rs779490893 |
| Gnomad | rs779490893 |
| Varsome | rs779490893 |
| LitVar | rs779490893 |
| Map | rs779490893 |
| PheGenI | rs779490893 |
| Biobank | rs779490893 |
| 1000 genomes | rs779490893 |
| hgdp | rs779490893 |
| ensembl | rs779490893 |
| geneview | rs779490893 |
| scholar | rs779490893 |
| rs779490893 | |
| pharmgkb | rs779490893 |
| gwascentral | rs779490893 |
| openSNP | rs779490893 |
| 23andMe | rs779490893 |
| SNPshot | rs779490893 |
| SNPdbe | rs779490893 |
| MSV3d | rs779490893 |
| GWAS Ctlg | rs779490893 |
| Max Magnitude | 0 |
aka NM_015512.4(DNAH1):c.11726_11727delCT or (p.Pro3909Argfs)
OMIM pathogenic variant
