rs28937891
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs28937891(G;T) |
| Make rs28937891(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 6301879 |
| Gene | WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28937891 |
| dbSNP (classic) | rs28937891 |
| ClinGen | rs28937891 |
| ebi | rs28937891 |
| HLI | rs28937891 |
| Exac | rs28937891 |
| Gnomad | rs28937891 |
| Varsome | rs28937891 |
| LitVar | rs28937891 |
| Map | rs28937891 |
| PheGenI | rs28937891 |
| Biobank | rs28937891 |
| 1000 genomes | rs28937891 |
| hgdp | rs28937891 |
| ensembl | rs28937891 |
| geneview | rs28937891 |
| scholar | rs28937891 |
| rs28937891 | |
| pharmgkb | rs28937891 |
| gwascentral | rs28937891 |
| openSNP | rs28937891 |
| 23andMe | rs28937891 |
| SNPshot | rs28937891 |
| SNPdbe | rs28937891 |
| MSV3d | rs28937891 |
| GWAS Ctlg | rs28937891 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28937891(A;A) rs28937891(T;T) |
| Alt | rs28937891(A;A) rs28937891(T;T) |
| Reference | Rs28937891(G;G) |
| Significance | Pathogenic |
| Disease | Diabetes mellitus AND insipidus with optic atrophy AND deafness |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | Diabetes mellitus AND insipidus with optic atrophy AND deafness |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6303606G>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000004768.5, |
