ENPP6
ectonucleotide pyrophosphatase/phosphodiesterase 6
Summary
Enables glycerophosphocholine cholinephosphodiesterase activity. Involved in choline metabolic process and lipid metabolic process. Located in extracellular region and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2476964398 | 4:185,012,370 | T/A | — | uncertain significance |
| rs376785932 | 4:185,012,404 | G/A | — | uncertain significance |
| rs775018210 | 4:185,012,454 | G/A | — | uncertain significance |
| rs2111323975 | 4:185,012,476 | A/G | — | uncertain significance |
| rs202227285 | 4:185,012,491 | C/T | — | uncertain significance |
| rs370136512 | 4:185,012,515 | C/G | — | uncertain significance |
| rs202045491 | 4:185,018,424 | C/T | — | uncertain significance |
| rs760745432 | 4:185,018,440 | C/T | — | uncertain significance |
| rs145892678 | 4:185,033,883 | T/C | — | uncertain significance |
| rs2477006279 | 4:185,033,911 | C/G | — | uncertain significance |
| rs150195560 | 4:185,033,920 | C/G | — | uncertain significance |
| rs754865458 | 4:185,033,952 | T/C | — | uncertain significance |
| rs748996220 | 4:185,038,026 | G/C | — | uncertain significance |
| rs377226218 | 4:185,038,129 | G/C | — | uncertain significance |
| rs778484221 | 4:185,038,176 | G/T | — | uncertain significance |
| rs151030639 | 4:185,038,943 | G/A | — | uncertain significance |
| rs1300734181 | 4:185,038,953 | C/T | — | uncertain significance |
| rs763550965 | 4:185,039,015 | C/T | — | uncertain significance |
| rs147979605 | 4:185,039,046 | G/A | — | uncertain significance |
| rs774846598 | 4:185,045,332 | T/A | — | uncertain significance |
| rs2477028995 | 4:185,045,395 | G/T | — | uncertain significance |
| rs17075332 | 4:185,059,939 | G/A | intron variant | — |
| rs79150573 | 4:185,059,985 | A/G | intron variant | — |
| rs368655804 | 4:185,074,698 | C/T | — | benign |
| rs776107487 | 4:185,074,731 | T/G | — | uncertain significance |
| rs750678862 | 4:185,074,754 | A/T | — | uncertain significance |
| rs937733501 | 4:185,074,795 | G/T | — | uncertain significance |
| rs2476827723 | 4:185,074,808 | A/G | — | uncertain significance |
| rs758733703 | 4:185,074,810 | G/A | — | likely benign |
| rs183023017 | 4:185,074,829 | T/G | — | uncertain significance |
| rs150523817 | 4:185,074,832 | G/T | missense variant | — |
| rs748938596 | 4:185,074,851 | A/G | — | uncertain significance |
| rs9994623 | 4:185,076,642 | G/C | intron variant | — |
| rs144581174 | 4:185,092,707 | G/A | intron variant | — |
| rs186086988 | 4:185,125,247 | C/T | intron variant | — |
| rs9312323 | 4:185,127,567 | G/C | intron variant | — |
| rs9312324 | 4:185,129,717 | A/T | — | — |
| rs201187797 | 4:185,131,886 | G/A | — | — |
| rs764447229 | 4:185,138,743 | G/T | — | uncertain significance |
| rs4861612 | 4:185,138,760 | C/T | — | benign |
| rs375419361 | 4:185,138,794 | A/C | — | uncertain significance |
| rs756834646 | 4:185,138,827 | C/G | — | uncertain significance |
| rs781237321 | 4:185,138,850 | A/C | — | uncertain significance |
| rs200037984 | 4:185,138,869 | C/A | — | uncertain significance |
| rs777264004 | 4:185,138,902 | C/T | — | uncertain significance |
| rs754840293 | 4:185,138,929 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.