rs190166486
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs190166486(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 80539915 |
| Gene | PTPRQ |
| is a | snp |
| is | mentioned by |
| dbSNP | rs190166486 |
| dbSNP (classic) | rs190166486 |
| ClinGen | rs190166486 |
| ebi | rs190166486 |
| HLI | rs190166486 |
| Exac | rs190166486 |
| Gnomad | rs190166486 |
| Varsome | rs190166486 |
| LitVar | rs190166486 |
| Map | rs190166486 |
| PheGenI | rs190166486 |
| Biobank | rs190166486 |
| 1000 genomes | rs190166486 |
| hgdp | rs190166486 |
| ensembl | rs190166486 |
| geneview | rs190166486 |
| scholar | rs190166486 |
| rs190166486 | |
| pharmgkb | rs190166486 |
| gwascentral | rs190166486 |
| openSNP | rs190166486 |
| 23andMe | rs190166486 |
| SNPshot | rs190166486 |
| SNPdbe | rs190166486 |
| MSV3d | rs190166486 |
| GWAS Ctlg | rs190166486 |
| Max Magnitude | 0 |
The rare allele for this PTPRQ gene variant is reported to be causative for a recessive form of deafness; see PTPRQ for details and sources.
