rs149013740
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs149013740(A;A) |
| Make rs149013740(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 4 |
| Position | 6301990 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs149013740 |
| dbSNP (classic) | rs149013740 |
| ClinGen | rs149013740 |
| ebi | rs149013740 |
| HLI | rs149013740 |
| Exac | rs149013740 |
| Gnomad | rs149013740 |
| Varsome | rs149013740 |
| LitVar | rs149013740 |
| Map | rs149013740 |
| PheGenI | rs149013740 |
| Biobank | rs149013740 |
| 1000 genomes | rs149013740 |
| hgdp | rs149013740 |
| ensembl | rs149013740 |
| geneview | rs149013740 |
| scholar | rs149013740 |
| rs149013740 | |
| pharmgkb | rs149013740 |
| gwascentral | rs149013740 |
| openSNP | rs149013740 |
| 23andMe | rs149013740 |
| SNPshot | rs149013740 |
| SNPdbe | rs149013740 |
| MSV3d | rs149013740 |
| GWAS Ctlg | rs149013740 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs149013740(A;A) |
| Alt | rs149013740(A;A) |
| Reference | Rs149013740(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided not specified |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | not provided not specified |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6303717G>A |
| CLNSRC | |
| CLNACC | RCV000197209.1, RCV000379222.1, |
