GPCPD1
glycerophosphocholine phosphodiesterase 1
Summary
Predicted to enable glycerophosphocholine phosphodiesterase activity. Predicted to be involved in glycerophospholipid catabolic process. Predicted to act upstream of or within skeletal muscle tissue development. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs752260906 | 20:5,528,321 | C/T | — | uncertain significance |
| rs140687246 | 20:5,528,386 | C/T | — | likely benign |
| rs146963061 | 20:5,528,440 | C/T | — | uncertain significance |
| rs185880154 | 20:5,528,441 | G/A | — | uncertain significance |
| rs761448888 | 20:5,538,640 | T/C | — | uncertain significance |
| rs1985874042 | 20:5,538,651 | T/C | — | uncertain significance |
| rs762561137 | 20:5,538,705 | A/C | — | uncertain significance |
| rs141677622 | 20:5,539,365 | T/C | — | uncertain significance |
| rs1179447177 | 20:5,539,371 | T/C | — | uncertain significance |
| rs1427379636 | 20:5,539,403 | T/A | — | uncertain significance |
| rs1282365216 | 20:5,542,161 | G/C | — | uncertain significance |
| rs11087685 | 20:5,544,987 | C/G | — | — |
| rs895539398 | 20:5,548,146 | G/T | — | uncertain significance |
| rs2515400886 | 20:5,548,202 | A/G | — | uncertain significance |
| rs755662 | 20:5,550,618 | A/T | intron variant | — |
| rs761860780 | 20:5,554,592 | G/C | — | uncertain significance |
| rs1490591594 | 20:5,556,563 | C/T | — | uncertain significance |
| rs144531830 | 20:5,556,596 | C/T | — | uncertain significance |
| rs772415258 | 20:5,559,076 | T/C | — | uncertain significance |
| rs376370791 | 20:5,559,204 | G/C | — | uncertain significance |
| rs150734510 | 20:5,559,221 | G/A | — | benign |
| rs766466152 | 20:5,566,862 | T/C | — | likely benign |
| rs543014162 | 20:5,566,910 | G/C | — | uncertain significance |
| rs2515469849 | 20:5,579,380 | G/A | — | uncertain significance |
| rs774827192 | 20:5,579,396 | G/T | — | uncertain significance |
| rs1426830136 | 20:5,579,452 | A/G | — | uncertain significance |
| rs142917605 | 20:5,579,454 | C/T | — | likely benign |
| rs73075609 | 20:5,580,789 | C/T | intron variant | — |
| rs238295 | 20:5,588,449 | A/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.