rs1046320
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs1046320(A;A) |
| Make rs1046320(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 6302617 |
| Gene | LOC107986257, WFS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1046320 |
| dbSNP (classic) | rs1046320 |
| ClinGen | rs1046320 |
| ebi | rs1046320 |
| HLI | rs1046320 |
| Exac | rs1046320 |
| Gnomad | rs1046320 |
| Varsome | rs1046320 |
| LitVar | rs1046320 |
| Map | rs1046320 |
| PheGenI | rs1046320 |
| Biobank | rs1046320 |
| 1000 genomes | rs1046320 |
| hgdp | rs1046320 |
| ensembl | rs1046320 |
| geneview | rs1046320 |
| scholar | rs1046320 |
| rs1046320 | |
| pharmgkb | rs1046320 |
| gwascentral | rs1046320 |
| openSNP | rs1046320 |
| 23andMe | rs1046320 |
| SNPshot | rs1046320 |
| SNPdbe | rs1046320 |
| MSV3d | rs1046320 |
| GWAS Ctlg | rs1046320 |
| GMAF | 0.3618 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20028947
] Detailed investigation of the role of common and low frequency WFS1 variants in type 2 diabetes risk
| ClinVar | |
|---|---|
| Risk | rs1046320(A;A) rs1046320(T;T) |
| Alt | rs1046320(A;A) rs1046320(T;T) |
| Reference | Rs1046320(G;G) |
| Significance | Non-pathogenic |
| Disease | Nonsyndromic Hearing Loss WFS1-Related Spectrum Disorders |
| Variation | info |
| Gene | WFS1 |
| CLNDBN | Nonsyndromic Hearing Loss, Dominant WFS1-Related Spectrum Disorders |
| Reversed | 0 |
| HGVS | NC_000004.11:g.6304344G>A |
| CLNSRC | |
| CLNACC | RCV000317741.1, RCV000356153.1, |
[PMID 29988211] Association of CpG-SNP and 3'UTR-SNP of WFS1 with the Risk of Type 2 Diabetes Mellitus in an Iranian Population.
