rs142668478
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs142668478(A;A) |
| Make rs142668478(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 6301849 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs142668478 |
| dbSNP (classic) | rs142668478 |
| ClinGen | rs142668478 |
| ebi | rs142668478 |
| HLI | rs142668478 |
| Exac | rs142668478 |
| Gnomad | rs142668478 |
| Varsome | rs142668478 |
| LitVar | rs142668478 |
| Map | rs142668478 |
| PheGenI | rs142668478 |
| Biobank | rs142668478 |
| 1000 genomes | rs142668478 |
| hgdp | rs142668478 |
| ensembl | rs142668478 |
| geneview | rs142668478 |
| scholar | rs142668478 |
| rs142668478 | |
| pharmgkb | rs142668478 |
| gwascentral | rs142668478 |
| openSNP | rs142668478 |
| 23andMe | rs142668478 |
| SNPshot | rs142668478 |
| SNPdbe | rs142668478 |
| MSV3d | rs142668478 |
| GWAS Ctlg | rs142668478 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs142668478(A;A) rs142668478(C;C) |
| Alt | rs142668478(A;A) rs142668478(C;C) |
| Reference | Rs142668478(G;G) |
| Significance | Pathogenic |
| Disease | not specified WFS1-Related Disorders |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not specified WFS1-Related Disorders |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6303576G>A; NC_000004.11:g.6303576G>C |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000198254.3, RCV000038650.2, |
