rs672601333
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs672601333(-;T) |
| Make rs672601333(T;T) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 5 |
| Position | 13894819 |
| Gene | DNAH5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs672601333 |
| dbSNP (classic) | rs672601333 |
| ClinGen | rs672601333 |
| ebi | rs672601333 |
| HLI | rs672601333 |
| Exac | rs672601333 |
| Gnomad | rs672601333 |
| Varsome | rs672601333 |
| LitVar | rs672601333 |
| Map | rs672601333 |
| PheGenI | rs672601333 |
| Biobank | rs672601333 |
| 1000 genomes | rs672601333 |
| hgdp | rs672601333 |
| ensembl | rs672601333 |
| geneview | rs672601333 |
| scholar | rs672601333 |
| rs672601333 | |
| pharmgkb | rs672601333 |
| gwascentral | rs672601333 |
| openSNP | rs672601333 |
| 23andMe | rs672601333 |
| SNPshot | rs672601333 |
| SNPdbe | rs672601333 |
| MSV3d | rs672601333 |
| GWAS Ctlg | rs672601333 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs672601333(T;T) |
| Alt | rs672601333(T;T) |
| Reference | Rs672601333(-;-) |
| Significance | Pathogenic |
| Disease | Ciliary dyskinesia |
| Variation | info |
| Gene | DNAH5 |
| CLNDBN | Ciliary dyskinesia, primary, 3 |
| Reversed | 1 |
| HGVS | NC_000005.9:g.13894929dupA |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000032853.5, |
