rs575017579
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs575017579(A;A) |
| Make rs575017579(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 5 |
| Position | 13840968 |
| Gene | DNAH5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs575017579 |
| dbSNP (classic) | rs575017579 |
| ClinGen | rs575017579 |
| ebi | rs575017579 |
| HLI | rs575017579 |
| Exac | rs575017579 |
| Gnomad | rs575017579 |
| Varsome | rs575017579 |
| LitVar | rs575017579 |
| Map | rs575017579 |
| PheGenI | rs575017579 |
| Biobank | rs575017579 |
| 1000 genomes | rs575017579 |
| hgdp | rs575017579 |
| ensembl | rs575017579 |
| geneview | rs575017579 |
| scholar | rs575017579 |
| rs575017579 | |
| pharmgkb | rs575017579 |
| gwascentral | rs575017579 |
| openSNP | rs575017579 |
| 23andMe | rs575017579 |
| SNPshot | rs575017579 |
| SNPdbe | rs575017579 |
| MSV3d | rs575017579 |
| GWAS Ctlg | rs575017579 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs575017579(A;A) rs575017579(C;C) |
| Alt | rs575017579(A;A) rs575017579(C;C) |
| Reference | Rs575017579(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | DNAH5 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.13841077G>A |
| CLNSRC | |
| CLNACC | RCV000494045.1, |
