rs760574657
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs760574657(C;T) |
| Make rs760574657(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 11 |
| Position | 121168903 |
| Gene | TECTA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs760574657 |
| dbSNP (classic) | rs760574657 |
| ClinGen | rs760574657 |
| ebi | rs760574657 |
| HLI | rs760574657 |
| Exac | rs760574657 |
| Gnomad | rs760574657 |
| Varsome | rs760574657 |
| LitVar | rs760574657 |
| Map | rs760574657 |
| PheGenI | rs760574657 |
| Biobank | rs760574657 |
| 1000 genomes | rs760574657 |
| hgdp | rs760574657 |
| ensembl | rs760574657 |
| geneview | rs760574657 |
| scholar | rs760574657 |
| rs760574657 | |
| pharmgkb | rs760574657 |
| gwascentral | rs760574657 |
| openSNP | rs760574657 |
| 23andMe | rs760574657 |
| SNPshot | rs760574657 |
| SNPdbe | rs760574657 |
| MSV3d | rs760574657 |
| GWAS Ctlg | rs760574657 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs760574657(T;T) |
| Alt | rs760574657(T;T) |
| Reference | Rs760574657(C;C) |
| Significance | Pathogenic |
| Disease | Nonsyndromic hearing loss and deafness |
| Variation | info |
| Gene | TECTA |
| CLNDBN | Nonsyndromic hearing loss and deafness |
| Reversed | 0 |
| HGVS | NC_000011.9:g.121039612C>T |
| CLNSRC | |
| CLNACC | RCV000220688.1, |
