rs370609551
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs370609551(A;A) |
| Make rs370609551(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 26474532 |
| Gene | OTOF |
| is a | snp |
| is | mentioned by |
| dbSNP | rs370609551 |
| dbSNP (classic) | rs370609551 |
| ClinGen | rs370609551 |
| ebi | rs370609551 |
| HLI | rs370609551 |
| Exac | rs370609551 |
| Gnomad | rs370609551 |
| Varsome | rs370609551 |
| LitVar | rs370609551 |
| Map | rs370609551 |
| PheGenI | rs370609551 |
| Biobank | rs370609551 |
| 1000 genomes | rs370609551 |
| hgdp | rs370609551 |
| ensembl | rs370609551 |
| geneview | rs370609551 |
| scholar | rs370609551 |
| rs370609551 | |
| pharmgkb | rs370609551 |
| gwascentral | rs370609551 |
| openSNP | rs370609551 |
| 23andMe | rs370609551 |
| SNPshot | rs370609551 |
| SNPdbe | rs370609551 |
| MSV3d | rs370609551 |
| GWAS Ctlg | rs370609551 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs370609551(A;A) rs370609551(T;T) |
| Alt | rs370609551(A;A) rs370609551(T;T) |
| Reference | Rs370609551(G;G) |
| Significance | Pathogenic |
| Disease | Deafness |
| Variation | info |
| Gene | OTOF |
| CLNDBN | Deafness, autosomal recessive 9 |
| Reversed | 0 |
| HGVS | NC_000002.11:g.26697400G>T |
| CLNSRC | ClinVar GeneReviews |
| CLNACC | RCV000056036.1, |
