PGM2L1
phosphoglucomutase 2 like 1
Summary
Enables glucose-1,6-bisphosphate synthase activity. Predicted to be involved in glucose metabolic process. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1044782 | 11:74,047,683 | A/G | — | benign |
| rs3867270 | 11:74,049,569 | A/G | — | benign |
| rs534083778 | 11:74,049,624 | C/T | — | uncertain significance |
| rs77817589 | 11:74,049,808 | A/G | — | benign |
| rs592644 | 11:74,053,547 | T/C | — | benign |
| rs138854022 | 11:74,053,552 | C/T | — | uncertain significance |
| rs371880752 | 11:74,053,553 | G/A | — | uncertain significance |
| rs146960261 | 11:74,053,573 | G/A | — | likely benign |
| rs369829875 | 11:74,053,620 | C/A | — | uncertain significance |
| rs75415490 | 11:74,054,175 | A/G | — | benign |
| rs641271 | 11:74,054,346 | G/T | — | benign |
| rs199706907 | 11:74,054,370 | A/G | — | uncertain significance |
| rs2495900037 | 11:74,054,377 | C/A | — | pathogenic |
| rs767118518 | 11:74,054,398 | C/A | — | pathogenic |
| rs7129306 | 11:74,057,355 | A/C | intron variant | — |
| rs519083 | 11:74,057,647 | T/C | — | benign |
| rs755037833 | 11:74,057,787 | G/A | — | uncertain significance |
| rs772571971 | 11:74,057,812 | A/C | — | uncertain significance |
| rs3741130 | 11:74,057,931 | C/T | — | benign |
| rs2495910569 | 11:74,058,248 | T/C | — | uncertain significance |
| rs2495918677 | 11:74,062,442 | C/A | — | uncertain significance |
| rs2495918820 | 11:74,062,467 | C/T | — | likely benign |
| rs754688887 | 11:74,062,536 | T/C | — | uncertain significance |
| rs10793077 | 11:74,062,821 | C/T | — | benign |
| rs11236077 | 11:74,079,475 | A/G | — | benign |
| rs143622830 | 11:74,079,500 | C/T | — | benign |
| rs763285642 | 11:74,081,993 | T/C | — | uncertain significance |
| rs560814 | 11:74,082,611 | T/G | — | benign |
| rs60942292 | 11:74,082,726 | A/G | — | benign |
| rs199926066 | 11:74,082,786 | C/A | — | uncertain significance |
| rs1462132853 | 11:74,082,789 | C/T | — | uncertain significance |
| rs201275731 | 11:74,082,832 | A/G | — | uncertain significance |
| rs61288268 | 11:74,085,384 | C/T | — | benign |
| rs35170680 | 11:74,085,420 | T/G | — | benign |
| rs1452899724 | 11:74,085,567 | G/A | — | pathogenic |
| rs59325091 | 11:74,094,498 | T/G | intron variant | — |
| rs11236096 | 11:74,108,950 | G/A | — | benign |
| rs12049823 | 11:74,109,166 | A/G | — | benign |
| rs148003019 | 11:74,109,178 | T/G | — | uncertain significance |
| rs988401745 | 11:74,109,188 | C/T | — | uncertain significance |
| rs78431863 | 11:74,109,553 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.