rs56002719
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs56002719(A;T) |
| Make rs56002719(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 6302122 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs56002719 |
| dbSNP (classic) | rs56002719 |
| ClinGen | rs56002719 |
| ebi | rs56002719 |
| HLI | rs56002719 |
| Exac | rs56002719 |
| Gnomad | rs56002719 |
| Varsome | rs56002719 |
| LitVar | rs56002719 |
| Map | rs56002719 |
| PheGenI | rs56002719 |
| Biobank | rs56002719 |
| 1000 genomes | rs56002719 |
| hgdp | rs56002719 |
| ensembl | rs56002719 |
| geneview | rs56002719 |
| scholar | rs56002719 |
| rs56002719 | |
| pharmgkb | rs56002719 |
| gwascentral | rs56002719 |
| openSNP | rs56002719 |
| 23andMe | rs56002719 |
| SNPshot | rs56002719 |
| SNPdbe | rs56002719 |
| MSV3d | rs56002719 |
| GWAS Ctlg | rs56002719 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs56002719(T;T) |
| Alt | rs56002719(T;T) |
| Reference | Rs56002719(A;A) |
| Significance | Other |
| Disease | not specified WFS1-Related Spectrum Disorders |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not specified WFS1-Related Spectrum Disorders |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6303849A>T |
| CLNSRC | |
| CLNACC | RCV000152695.3, RCV000351538.1, |
