rs904944428
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (-;-) | 0 | common in clinvar |
| Make rs904944428(-;T) |
| Make rs904944428(T;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 6 |
| Position | 24301742 |
| Gene | DCDC2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs904944428 |
| dbSNP (classic) | rs904944428 |
| ClinGen | rs904944428 |
| ebi | rs904944428 |
| HLI | rs904944428 |
| Exac | rs904944428 |
| Gnomad | rs904944428 |
| Varsome | rs904944428 |
| LitVar | rs904944428 |
| Map | rs904944428 |
| PheGenI | rs904944428 |
| Biobank | rs904944428 |
| 1000 genomes | rs904944428 |
| hgdp | rs904944428 |
| ensembl | rs904944428 |
| geneview | rs904944428 |
| scholar | rs904944428 |
| rs904944428 | |
| pharmgkb | rs904944428 |
| gwascentral | rs904944428 |
| openSNP | rs904944428 |
| 23andMe | rs904944428 |
| SNPshot | rs904944428 |
| SNPdbe | rs904944428 |
| MSV3d | rs904944428 |
| GWAS Ctlg | rs904944428 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs904944428(T;T) |
| Alt | rs904944428(T;T) |
| Reference | Rs904944428(-;-) |
| Significance | Pathogenic |
| Disease | Sclerosing cholangitis |
| Variation | info |
| Gene | DCDC2 |
| CLNDBN | Sclerosing cholangitis, neonatal |
| Reversed | 0 |
| HGVS | NC_000006.11:g.24301971dup |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000477740.1, |
