CHPF2
chondroitin polymerizing factor 2
Summary
Predicted to enable glucuronosyl-N-acetylgalactosaminyl-proteoglycan 4-beta-N-acetylgalactosaminyltransferase activity. Located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants63 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs772517432 | 7:150,931,102 | G/A | — | uncertain significance |
| rs761779746 | 7:150,931,227 | G/C | — | uncertain significance |
| rs868462953 | 7:150,931,234 | T/C | — | uncertain significance |
| rs781686805 | 7:150,931,272 | G/A | — | likely benign |
| rs746152043 | 7:150,931,275 | C/T | — | uncertain significance |
| rs1374373933 | 7:150,931,343 | C/T | — | likely benign |
| rs111632177 | 7:150,931,805 | G/A | downstream gene variant | — |
| rs540455097 | 7:150,932,165 | C/T | — | uncertain significance |
| rs1019643191 | 7:150,932,210 | T/C | — | uncertain significance |
| rs138209627 | 7:150,932,222 | G/A | — | uncertain significance |
| rs781132727 | 7:150,932,283 | G/T | — | uncertain significance |
| rs771016614 | 7:150,932,381 | T/G | — | uncertain significance |
| rs776746591 | 7:150,932,382 | T/C | — | uncertain significance |
| rs573329006 | 7:150,932,391 | A/G | — | uncertain significance |
| rs756908856 | 7:150,932,401 | G/T | — | uncertain significance |
| rs2485786569 | 7:150,932,439 | C/T | — | uncertain significance |
| rs200727358 | 7:150,932,511 | T/C | — | uncertain significance |
| rs753786949 | 7:150,932,516 | G/A | — | uncertain significance |
| rs372526283 | 7:150,932,522 | G/A | — | uncertain significance |
| rs781339177 | 7:150,932,531 | C/T | — | uncertain significance |
| rs148527739 | 7:150,932,532 | G/A | — | uncertain significance |
| rs769832181 | 7:150,932,538 | G/C | — | uncertain significance |
| rs200719651 | 7:150,932,589 | G/A | — | uncertain significance |
| rs117332591 | 7:150,932,631 | A/G | — | benign |
| rs764831627 | 7:150,932,651 | C/T | — | uncertain significance |
| rs367594969 | 7:150,932,661 | T/C | — | uncertain significance |
| rs199940789 | 7:150,932,678 | G/A | — | uncertain significance |
| rs1302500978 | 7:150,932,679 | G/A | — | uncertain significance |
| rs774233185 | 7:150,933,531 | G/C | — | uncertain significance |
| rs150602051 | 7:150,933,574 | C/T | — | likely benign |
| rs141615629 | 7:150,934,470 | G/A | — | uncertain significance |
| rs1013133945 | 7:150,934,503 | C/G | — | uncertain significance |
| rs139379425 | 7:150,934,562 | G/T | — | uncertain significance |
| rs548114993 | 7:150,934,655 | G/A | — | uncertain significance |
| rs368166726 | 7:150,934,665 | C/T | — | uncertain significance |
| rs147884296 | 7:150,934,669 | A/G | — | likely benign |
| rs375493278 | 7:150,934,694 | C/T | — | uncertain significance |
| rs988681298 | 7:150,934,698 | G/A | — | uncertain significance |
| rs746382000 | 7:150,934,710 | G/A | — | uncertain significance |
| rs764967022 | 7:150,934,746 | A/C | — | uncertain significance |
| rs140251502 | 7:150,934,749 | G/A | — | uncertain significance |
| rs768923356 | 7:150,934,757 | G/A | — | uncertain significance |
| rs774798247 | 7:150,934,767 | G/A | — | uncertain significance |
| rs747805127 | 7:150,934,772 | A/T | — | uncertain significance |
| rs759463177 | 7:150,934,799 | G/C | — | uncertain significance |
| rs767776711 | 7:150,934,813 | G/C | — | uncertain significance |
| rs144589067 | 7:150,934,827 | G/A | — | likely benign |
| rs370642310 | 7:150,934,911 | G/A | — | uncertain significance |
| rs968620779 | 7:150,934,920 | T/C | — | uncertain significance |
| rs375138900 | 7:150,934,937 | G/A | — | uncertain significance |
| rs777022105 | 7:150,935,036 | G/A | — | uncertain significance |
| rs751982524 | 7:150,935,055 | G/A | — | uncertain significance |
| rs1327280036 | 7:150,935,178 | T/C | — | uncertain significance |
| rs142607366 | 7:150,935,271 | G/A | — | uncertain significance |
| rs140898729 | 7:150,935,328 | A/G | — | uncertain significance |
| rs563493546 | 7:150,935,384 | C/G | — | uncertain significance |
| rs542748933 | 7:150,935,414 | C/T | — | uncertain significance |
| rs146697508 | 7:150,935,501 | C/T | — | uncertain significance |
| rs747755752 | 7:150,935,600 | C/T | — | uncertain significance |
| rs1233772650 | 7:150,935,640 | G/A | — | uncertain significance |
| rs1427875778 | 7:150,935,709 | G/A | — | uncertain significance |
| rs371871987 | 7:150,935,735 | C/G | — | uncertain significance |
| rs760750092 | 7:150,935,741 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.