rs141585847
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs141585847(G;G) |
| Make rs141585847(G;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 6301111 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs141585847 |
| dbSNP (classic) | rs141585847 |
| ClinGen | rs141585847 |
| ebi | rs141585847 |
| HLI | rs141585847 |
| Exac | rs141585847 |
| Gnomad | rs141585847 |
| Varsome | rs141585847 |
| LitVar | rs141585847 |
| Map | rs141585847 |
| PheGenI | rs141585847 |
| Biobank | rs141585847 |
| 1000 genomes | rs141585847 |
| hgdp | rs141585847 |
| ensembl | rs141585847 |
| geneview | rs141585847 |
| scholar | rs141585847 |
| rs141585847 | |
| pharmgkb | rs141585847 |
| gwascentral | rs141585847 |
| openSNP | rs141585847 |
| 23andMe | rs141585847 |
| SNPshot | rs141585847 |
| SNPdbe | rs141585847 |
| MSV3d | rs141585847 |
| GWAS Ctlg | rs141585847 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs141585847(G;G) |
| Alt | rs141585847(G;G) |
| Reference | Rs141585847(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6302838T>G |
| CLNSRC | |
| CLNACC | RCV000199551.1, |
