rs201306709
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs201306709(A;A) |
| Make rs201306709(A;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 12 |
| Position | 65368997 |
| Gene | MSRB3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201306709 |
| dbSNP (classic) | rs201306709 |
| ClinGen | rs201306709 |
| ebi | rs201306709 |
| HLI | rs201306709 |
| Exac | rs201306709 |
| Gnomad | rs201306709 |
| Varsome | rs201306709 |
| LitVar | rs201306709 |
| Map | rs201306709 |
| PheGenI | rs201306709 |
| Biobank | rs201306709 |
| 1000 genomes | rs201306709 |
| hgdp | rs201306709 |
| ensembl | rs201306709 |
| geneview | rs201306709 |
| scholar | rs201306709 |
| rs201306709 | |
| pharmgkb | rs201306709 |
| gwascentral | rs201306709 |
| openSNP | rs201306709 |
| 23andMe | rs201306709 |
| SNPshot | rs201306709 |
| SNPdbe | rs201306709 |
| MSV3d | rs201306709 |
| GWAS Ctlg | rs201306709 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201306709(A;A) |
| Alt | rs201306709(A;A) |
| Reference | Rs201306709(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Nonsyndromic hearing loss and deafness |
| Variation | info |
| Gene | MSRB3 |
| CLNDBN | Nonsyndromic hearing loss and deafness |
| Reversed | 0 |
| HGVS | NC_000012.11:g.65762777G>A |
| CLNSRC | |
| CLNACC | RCV000216815.1, |
