rs113446173
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs113446173(G;T) |
| Make rs113446173(T;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 6301166 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs113446173 |
| dbSNP (classic) | rs113446173 |
| ClinGen | rs113446173 |
| ebi | rs113446173 |
| HLI | rs113446173 |
| Exac | rs113446173 |
| Gnomad | rs113446173 |
| Varsome | rs113446173 |
| LitVar | rs113446173 |
| Map | rs113446173 |
| PheGenI | rs113446173 |
| Biobank | rs113446173 |
| 1000 genomes | rs113446173 |
| hgdp | rs113446173 |
| ensembl | rs113446173 |
| geneview | rs113446173 |
| scholar | rs113446173 |
| rs113446173 | |
| pharmgkb | rs113446173 |
| gwascentral | rs113446173 |
| openSNP | rs113446173 |
| 23andMe | rs113446173 |
| SNPshot | rs113446173 |
| SNPdbe | rs113446173 |
| MSV3d | rs113446173 |
| GWAS Ctlg | rs113446173 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs113446173(T;T) |
| Alt | rs113446173(T;T) |
| Reference | Rs113446173(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6302893G>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000488089.1, |
