PTCHD4
patched domain containing 4
Summary
Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6933704 | 6:47,844,469 | G/A | downstream gene variant | — |
| rs148669879 | 6:47,846,110 | T/C | — | uncertain significance |
| rs142142059 | 6:47,846,125 | T/C | — | uncertain significance |
| rs754669023 | 6:47,846,233 | T/C | — | uncertain significance |
| rs2533140346 | 6:47,846,331 | C/T | — | uncertain significance |
| rs146541117 | 6:47,846,403 | A/G | — | uncertain significance |
| rs779059101 | 6:47,846,455 | C/G | — | uncertain significance |
| rs1414208553 | 6:47,846,469 | G/A | — | uncertain significance |
| rs1763921999 | 6:47,846,535 | G/A | — | uncertain significance |
| rs781412213 | 6:47,846,581 | C/T | — | uncertain significance |
| rs774846973 | 6:47,846,610 | A/G | — | uncertain significance |
| rs550307277 | 6:47,846,627 | G/T | — | uncertain significance |
| rs766408254 | 6:47,846,632 | T/C | — | uncertain significance |
| rs763733920 | 6:47,846,733 | C/T | — | uncertain significance |
| rs749476071 | 6:47,846,761 | G/A | — | uncertain significance |
| rs910334387 | 6:47,846,815 | G/C | — | uncertain significance |
| rs2533143503 | 6:47,846,860 | C/T | — | uncertain significance |
| rs1763939275 | 6:47,846,887 | C/T | — | uncertain significance |
| rs1334349638 | 6:47,846,959 | G/A | — | uncertain significance |
| rs746044962 | 6:47,847,013 | C/T | — | likely benign |
| rs372990137 | 6:47,847,180 | A/G | — | uncertain significance |
| rs1763952879 | 6:47,847,210 | C/A | — | uncertain significance |
| rs749315183 | 6:47,847,259 | A/G | — | uncertain significance |
| rs768483547 | 6:47,847,304 | T/C | — | uncertain significance |
| rs371091755 | 6:47,847,331 | G/A | — | uncertain significance |
| rs139641046 | 6:47,847,370 | T/C | — | uncertain significance |
| rs955700510 | 6:47,847,468 | A/G | — | uncertain significance |
| rs190905682 | 6:47,847,600 | T/C | — | uncertain significance |
| rs146439222 | 6:47,876,172 | T/C | intron variant | — |
| rs12209128 | 6:47,882,548 | T/C | — | — |
| rs76796948 | 6:47,946,757 | C/A | — | — |
| rs764290150 | 6:47,976,385 | G/T | — | uncertain significance |
| rs1342040351 | 6:47,976,402 | G/A | — | uncertain significance |
| rs375507616 | 6:47,976,481 | G/A | — | uncertain significance |
| rs758148370 | 6:47,976,602 | G/T | — | uncertain significance |
| rs771173497 | 6:47,976,650 | A/T | — | uncertain significance |
| rs1484037883 | 6:47,976,658 | C/T | — | uncertain significance |
| rs761256518 | 6:47,976,679 | T/C | — | uncertain significance |
| rs45461096 | 6:47,976,708 | A/G | — | uncertain significance |
| rs771245624 | 6:47,976,763 | C/T | — | uncertain significance |
| rs2533034954 | 6:47,976,788 | T/G | — | uncertain significance |
| rs1257007645 | 6:48,036,010 | C/T | — | uncertain significance |
| rs780191656 | 6:48,036,024 | T/C | — | uncertain significance |
| rs776348743 | 6:48,036,105 | T/C | — | uncertain significance |
| rs917465865 | 6:48,036,120 | A/G | — | uncertain significance |
| rs1286293810 | 6:48,036,165 | G/A | — | uncertain significance |
| rs546524803 | 6:48,036,175 | G/C | — | uncertain significance |
| rs2481056256 | 6:48,036,190 | C/G | — | uncertain significance |
| rs780659610 | 6:48,036,194 | G/C | — | likely benign |
| rs777537625 | 6:48,036,273 | C/T | — | uncertain significance |
| rs1041272848 | 6:48,036,283 | A/C | — | uncertain significance |
| rs1377032307 | 6:48,036,372 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.