rs749210663
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs749210663(-;-) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 80669467 |
| Gene | LOC105369867, PTPRQ |
| is a | snp |
| is | mentioned by |
| dbSNP | rs749210663 |
| dbSNP (classic) | rs749210663 |
| ClinGen | rs749210663 |
| ebi | rs749210663 |
| HLI | rs749210663 |
| Exac | rs749210663 |
| Gnomad | rs749210663 |
| Varsome | rs749210663 |
| LitVar | rs749210663 |
| Map | rs749210663 |
| PheGenI | rs749210663 |
| Biobank | rs749210663 |
| 1000 genomes | rs749210663 |
| hgdp | rs749210663 |
| ensembl | rs749210663 |
| geneview | rs749210663 |
| scholar | rs749210663 |
| rs749210663 | |
| pharmgkb | rs749210663 |
| gwascentral | rs749210663 |
| openSNP | rs749210663 |
| 23andMe | rs749210663 |
| SNPshot | rs749210663 |
| SNPdbe | rs749210663 |
| MSV3d | rs749210663 |
| GWAS Ctlg | rs749210663 |
| Max Magnitude | 0 |
The rare (deletion) allele for this PTPRQ gene variant is reported to be causative for a recessive form of deafness; see PTPRQ for details and sources.
