rs71537685
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs71537685(A;A) |
| Make rs71537685(A;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 4 |
| Position | 6300657 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs71537685 |
| dbSNP (classic) | rs71537685 |
| ClinGen | rs71537685 |
| ebi | rs71537685 |
| HLI | rs71537685 |
| Exac | rs71537685 |
| Gnomad | rs71537685 |
| Varsome | rs71537685 |
| LitVar | rs71537685 |
| Map | rs71537685 |
| PheGenI | rs71537685 |
| Biobank | rs71537685 |
| 1000 genomes | rs71537685 |
| hgdp | rs71537685 |
| ensembl | rs71537685 |
| geneview | rs71537685 |
| scholar | rs71537685 |
| rs71537685 | |
| pharmgkb | rs71537685 |
| gwascentral | rs71537685 |
| openSNP | rs71537685 |
| 23andMe | rs71537685 |
| SNPshot | rs71537685 |
| SNPdbe | rs71537685 |
| MSV3d | rs71537685 |
| GWAS Ctlg | rs71537685 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs71537685(A;A) |
| Alt | rs71537685(A;A) |
| Reference | Rs71537685(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6302384G>A |
| CLNSRC | |
| CLNACC | RCV000171514.2, |
