PRR22
proline rich 22
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs367836592 | 19:5,782,723 | G/A | — | — |
| rs2512704986 | 19:5,783,024 | C/G | — | uncertain significance |
| rs537666246 | 19:5,783,026 | G/A | — | uncertain significance |
| rs762760503 | 19:5,783,030 | G/C | — | uncertain significance |
| rs778379607 | 19:5,783,053 | G/T | — | uncertain significance |
| rs1304369933 | 19:5,783,098 | G/A | — | uncertain significance |
| rs1301071254 | 19:5,783,123 | G/C | — | uncertain significance |
| rs375221077 | 19:5,783,152 | G/A | — | uncertain significance |
| rs984426540 | 19:5,783,156 | G/A | — | uncertain significance |
| rs113531842 | 19:5,783,161 | G/A | — | uncertain significance |
| rs781426775 | 19:5,783,234 | C/T | — | uncertain significance |
| rs2512705467 | 19:5,783,255 | G/C | — | uncertain significance |
| rs759843689 | 19:5,783,278 | C/T | — | uncertain significance |
| rs148475602 | 19:5,783,288 | C/T | — | uncertain significance |
| rs757260642 | 19:5,783,369 | G/A | — | uncertain significance |
| rs773981799 | 19:5,783,416 | G/A | — | uncertain significance |
| rs889930683 | 19:5,783,474 | C/A | — | uncertain significance |
| rs1038408107 | 19:5,783,489 | C/T | — | uncertain significance |
| rs778215850 | 19:5,783,507 | T/C | — | uncertain significance |
| rs750123018 | 19:5,783,571 | G/T | — | uncertain significance |
| rs774634730 | 19:5,783,603 | C/T | — | likely benign |
| rs1247197333 | 19:5,783,669 | G/A | — | uncertain significance |
| rs1012676291 | 19:5,783,737 | G/A | — | uncertain significance |
| rs756628296 | 19:5,783,771 | C/T | — | uncertain significance |
| rs764732747 | 19:5,783,773 | T/C | — | uncertain significance |
| rs779480868 | 19:5,783,780 | C/A | — | uncertain significance |
| rs750655858 | 19:5,783,792 | C/T | — | uncertain significance |
| rs751819459 | 19:5,783,887 | G/T | — | uncertain significance |
| rs369088362 | 19:5,783,930 | C/T | — | uncertain significance |
| rs1434240145 | 19:5,783,944 | G/A | — | likely benign |
| rs766814720 | 19:5,783,954 | C/T | — | uncertain significance |
| rs2512706812 | 19:5,783,962 | G/A | — | uncertain significance |
| rs1227049689 | 19:5,784,447 | G/A | — | uncertain significance |
| rs375731438 | 19:5,784,545 | T/C | — | likely benign |
| rs370365763 | 19:5,784,560 | C/T | — | uncertain significance |
| rs543083484 | 19:5,784,655 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.