rs764153521
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs764153521(A;A) |
| Make rs764153521(A;C) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 121160302 |
| Gene | TECTA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs764153521 |
| dbSNP (classic) | rs764153521 |
| ClinGen | rs764153521 |
| ebi | rs764153521 |
| HLI | rs764153521 |
| Exac | rs764153521 |
| Gnomad | rs764153521 |
| Varsome | rs764153521 |
| LitVar | rs764153521 |
| Map | rs764153521 |
| PheGenI | rs764153521 |
| Biobank | rs764153521 |
| 1000 genomes | rs764153521 |
| hgdp | rs764153521 |
| ensembl | rs764153521 |
| geneview | rs764153521 |
| scholar | rs764153521 |
| rs764153521 | |
| pharmgkb | rs764153521 |
| gwascentral | rs764153521 |
| openSNP | rs764153521 |
| 23andMe | rs764153521 |
| SNPshot | rs764153521 |
| SNPdbe | rs764153521 |
| MSV3d | rs764153521 |
| GWAS Ctlg | rs764153521 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs764153521(A;A) rs764153521(T;T) |
| Alt | rs764153521(A;A) rs764153521(T;T) |
| Reference | Rs764153521(C;C) |
| Significance | Pathogenic |
| Disease | Deafness |
| Variation | info |
| Gene | TECTA |
| CLNDBN | Deafness, autosomal recessive 21 |
| Reversed | 0 |
| HGVS | NC_000011.9:g.121031011C>A |
| CLNSRC | |
| CLNACC | RCV000454140.1, |
