PGM2
phosphoglucomutase 2
Summary
Enables phosphoglucomutase activity and phosphopentomutase activity. Predicted to be involved in purine ribonucleoside salvage. Predicted to act upstream of or within glucose metabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants32 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1481330825 | 4:37,828,382 | G/C | — | uncertain significance |
| rs114326618 | 4:37,831,604 | G/A | — | benign |
| rs201598002 | 4:37,831,647 | G/A | — | likely benign |
| rs749686877 | 4:37,831,703 | G/A | — | uncertain significance |
| rs113769990 | 4:37,836,235 | T/C | — | likely benign |
| rs368241584 | 4:37,836,313 | G/A | — | uncertain significance |
| rs141644153 | 4:37,839,164 | G/A | — | uncertain significance |
| rs780181038 | 4:37,841,539 | G/A | — | uncertain significance |
| rs1395154874 | 4:37,841,691 | T/C | — | uncertain significance |
| rs770172003 | 4:37,841,824 | C/T | — | uncertain significance |
| rs749315628 | 4:37,841,839 | A/G | — | likely benign |
| rs779089658 | 4:37,846,004 | A/G | — | uncertain significance |
| rs764040395 | 4:37,846,043 | C/T | — | uncertain significance |
| rs1280867779 | 4:37,846,073 | T/C | — | uncertain significance |
| rs34893278 | 4:37,847,310 | C/T | — | benign |
| rs762388948 | 4:37,848,565 | G/T | — | uncertain significance |
| rs770928939 | 4:37,848,616 | T/C | — | uncertain significance |
| rs151106378 | 4:37,848,640 | C/T | — | uncertain significance |
| rs750473953 | 4:37,848,659 | C/T | — | uncertain significance |
| rs781317423 | 4:37,848,679 | G/A | — | uncertain significance |
| rs1487159797 | 4:37,848,698 | G/A | — | uncertain significance |
| rs1336209674 | 4:37,848,872 | T/C | — | uncertain significance |
| rs149127424 | 4:37,850,190 | G/A | — | uncertain significance |
| rs764267899 | 4:37,851,807 | A/G | — | uncertain significance |
| rs748345202 | 4:37,851,848 | G/A | — | uncertain significance |
| rs138782294 | 4:37,851,857 | A/G | — | uncertain significance |
| rs1316699139 | 4:37,851,894 | A/G | — | uncertain significance |
| rs35619511 | 4:37,853,557 | A/T | — | — |
| rs757501994 | 4:37,857,239 | C/G | — | uncertain significance |
| rs150524340 | 4:37,857,299 | G/A | — | uncertain significance |
| rs139469063 | 4:37,857,332 | A/G | missense variant | — |
| rs1726176108 | 4:37,857,349 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.