rs147499872
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs147499872(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 13916424 |
| Gene | DNAH5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs147499872 |
| dbSNP (classic) | rs147499872 |
| ClinGen | rs147499872 |
| ebi | rs147499872 |
| HLI | rs147499872 |
| Exac | rs147499872 |
| Gnomad | rs147499872 |
| Varsome | rs147499872 |
| LitVar | rs147499872 |
| Map | rs147499872 |
| PheGenI | rs147499872 |
| Biobank | rs147499872 |
| 1000 genomes | rs147499872 |
| hgdp | rs147499872 |
| ensembl | rs147499872 |
| geneview | rs147499872 |
| scholar | rs147499872 |
| rs147499872 | |
| pharmgkb | rs147499872 |
| gwascentral | rs147499872 |
| openSNP | rs147499872 |
| 23andMe | rs147499872 |
| SNPshot | rs147499872 |
| SNPdbe | rs147499872 |
| MSV3d | rs147499872 |
| GWAS Ctlg | rs147499872 |
| GMAF | 0.0004591 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs147499872(G;G) |
| Alt | rs147499872(G;G) |
| Reference | Rs147499872(A;A) |
| Significance | Pathogenic |
| Disease | Ciliary dyskinesia Primary ciliary dyskinesia |
| Variation | info |
| Gene | DNAH5 |
| CLNDBN | Ciliary dyskinesia, primary, 3 Primary ciliary dyskinesia |
| Reversed | 0 |
| HGVS | NC_000005.9:g.13916533A>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000032855.4, RCV000228082.3, |
