rs118204029
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs118204029(C;T) |
| Make rs118204029(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 37724918 |
| Gene | TRIOBP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs118204029 |
| dbSNP (classic) | rs118204029 |
| ClinGen | rs118204029 |
| ebi | rs118204029 |
| HLI | rs118204029 |
| Exac | rs118204029 |
| Gnomad | rs118204029 |
| Varsome | rs118204029 |
| LitVar | rs118204029 |
| Map | rs118204029 |
| PheGenI | rs118204029 |
| Biobank | rs118204029 |
| 1000 genomes | rs118204029 |
| hgdp | rs118204029 |
| ensembl | rs118204029 |
| geneview | rs118204029 |
| scholar | rs118204029 |
| rs118204029 | |
| pharmgkb | rs118204029 |
| gwascentral | rs118204029 |
| openSNP | rs118204029 |
| 23andMe | rs118204029 |
| SNPshot | rs118204029 |
| SNPdbe | rs118204029 |
| MSV3d | rs118204029 |
| GWAS Ctlg | rs118204029 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs118204029(T;T) |
| Alt | rs118204029(T;T) |
| Reference | Rs118204029(C;C) |
| Significance | Pathogenic |
| Disease | Deafness |
| Variation | info |
| Gene | TRIOBP |
| CLNDBN | Deafness, autosomal recessive 28 |
| Reversed | 0 |
| HGVS | NC_000022.10:g.38120925C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000001558.3, |
