rs397517865
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs397517865(C;C) |
| Make rs397517865(C;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 46705910 |
| Gene | TMIE |
| is a | snp |
| is | mentioned by |
| dbSNP | rs397517865 |
| dbSNP (classic) | rs397517865 |
| ClinGen | rs397517865 |
| ebi | rs397517865 |
| HLI | rs397517865 |
| Exac | rs397517865 |
| Gnomad | rs397517865 |
| Varsome | rs397517865 |
| LitVar | rs397517865 |
| Map | rs397517865 |
| PheGenI | rs397517865 |
| Biobank | rs397517865 |
| 1000 genomes | rs397517865 |
| hgdp | rs397517865 |
| ensembl | rs397517865 |
| geneview | rs397517865 |
| scholar | rs397517865 |
| rs397517865 | |
| pharmgkb | rs397517865 |
| gwascentral | rs397517865 |
| openSNP | rs397517865 |
| 23andMe | rs397517865 |
| SNPshot | rs397517865 |
| SNPdbe | rs397517865 |
| MSV3d | rs397517865 |
| GWAS Ctlg | rs397517865 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs397517865(A;A) rs397517865(C;C) |
| Alt | rs397517865(A;A) rs397517865(C;C) |
| Reference | Rs397517865(G;G) |
| Significance | Probable-Pathogenic |
| Disease | Nonsyndromic hearing loss and deafness |
| Variation | info |
| Gene | TMIE |
| CLNDBN | Nonsyndromic hearing loss and deafness |
| Reversed | 0 |
| HGVS | NC_000003.11:g.46747400G>C |
| CLNSRC | ClinVar |
| CLNACC | RCV000041229.2, |
