rs61729287
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common/normal |
| (C;T) | 3 | Carrier for a recessive mutation for deafness |
| Make rs61729287(C;G) |
| Make rs61729287(G;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 12 |
| Position | 80484531 |
| Gene | PTPRQ |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61729287 |
| dbSNP (classic) | rs61729287 |
| ClinGen | rs61729287 |
| ebi | rs61729287 |
| HLI | rs61729287 |
| Exac | rs61729287 |
| Gnomad | rs61729287 |
| Varsome | rs61729287 |
| LitVar | rs61729287 |
| Map | rs61729287 |
| PheGenI | rs61729287 |
| Biobank | rs61729287 |
| 1000 genomes | rs61729287 |
| hgdp | rs61729287 |
| ensembl | rs61729287 |
| geneview | rs61729287 |
| scholar | rs61729287 |
| rs61729287 | |
| pharmgkb | rs61729287 |
| gwascentral | rs61729287 |
| openSNP | rs61729287 |
| 23andMe | rs61729287 |
| SNPshot | rs61729287 |
| SNPdbe | rs61729287 |
| MSV3d | rs61729287 |
| GWAS Ctlg | rs61729287 |
| Max Magnitude | 3 |
The rare (T) allele for this PTPRQ gene variant is reported to be causative for a recessive form of deafness; see PTPRQ for details and sources.
