rs767561828
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs767561828(G;G) |
| Make rs767561828(G;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 6300990 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs767561828 |
| dbSNP (classic) | rs767561828 |
| ClinGen | rs767561828 |
| ebi | rs767561828 |
| HLI | rs767561828 |
| Exac | rs767561828 |
| Gnomad | rs767561828 |
| Varsome | rs767561828 |
| LitVar | rs767561828 |
| Map | rs767561828 |
| PheGenI | rs767561828 |
| Biobank | rs767561828 |
| 1000 genomes | rs767561828 |
| hgdp | rs767561828 |
| ensembl | rs767561828 |
| geneview | rs767561828 |
| scholar | rs767561828 |
| rs767561828 | |
| pharmgkb | rs767561828 |
| gwascentral | rs767561828 |
| openSNP | rs767561828 |
| 23andMe | rs767561828 |
| SNPshot | rs767561828 |
| SNPdbe | rs767561828 |
| MSV3d | rs767561828 |
| GWAS Ctlg | rs767561828 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs767561828(G;G) |
| Alt | rs767561828(G;G) |
| Reference | Rs767561828(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6302717T>G |
| CLNSRC | |
| CLNACC | RCV000195821.2, |
