rs111033256
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs111033256(A;A) |
| Make rs111033256(A;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 107675060 |
| Gene | SLC26A4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs111033256 |
| dbSNP (classic) | rs111033256 |
| ClinGen | rs111033256 |
| ebi | rs111033256 |
| HLI | rs111033256 |
| Exac | rs111033256 |
| Gnomad | rs111033256 |
| Varsome | rs111033256 |
| LitVar | rs111033256 |
| Map | rs111033256 |
| PheGenI | rs111033256 |
| Biobank | rs111033256 |
| 1000 genomes | rs111033256 |
| hgdp | rs111033256 |
| ensembl | rs111033256 |
| geneview | rs111033256 |
| scholar | rs111033256 |
| rs111033256 | |
| pharmgkb | rs111033256 |
| gwascentral | rs111033256 |
| openSNP | rs111033256 |
| 23andMe | rs111033256 |
| SNPshot | rs111033256 |
| SNPdbe | rs111033256 |
| MSV3d | rs111033256 |
| GWAS Ctlg | rs111033256 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs111033256(A;A) |
| Alt | rs111033256(A;A) |
| Reference | Rs111033256(T;T) |
| Significance | Other |
| Disease | Enlarged vestibular aqueduct syndrome Pendred's syndrome |
| Variation | info |
| Gene | SLC26A4 |
| CLNDBN | Enlarged vestibular aqueduct syndrome Pendred's syndrome |
| Reversed | 0 |
| HGVS | NC_000007.13:g.107315505T>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000036506.2, RCV000169244.3, |
[PMID 12676893
] Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
[PMID 12974744] Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.
[PMID 16460646] Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population.
