LHPP
phospholysine phosphohistidine inorganic pyrophosphate phosphatase
Summary
Enables inorganic diphosphate phosphatase activity and protein homodimerization activity. Involved in phosphate-containing compound metabolic process. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145709387 | 10:126,149,591 | A/T | upstream gene variant | — |
| rs376697964 | 10:126,150,302 | T/G | — | — |
| rs762295411 | 10:126,150,444 | G/A | — | uncertain significance |
| rs1293255607 | 10:126,150,456 | G/C | — | uncertain significance |
| rs75426652 | 10:126,150,523 | C/A | missense variant | — |
| rs1254139779 | 10:126,150,543 | G/C | — | uncertain significance |
| rs1196448228 | 10:126,150,544 | A/G | — | uncertain significance |
| rs1281389112 | 10:126,150,547 | C/T | — | uncertain significance |
| rs146134571 | 10:126,159,805 | C/G | regulatory region variant | — |
| rs61861927 | 10:126,160,495 | G/T | — | — |
| rs754601667 | 10:126,172,718 | T/C | — | uncertain significance |
| rs145463900 | 10:126,172,722 | G/A | — | uncertain significance |
| rs2494749261 | 10:126,172,739 | T/C | — | uncertain significance |
| rs200583242 | 10:126,172,764 | G/A | — | uncertain significance |
| rs376421647 | 10:126,172,782 | A/G | — | uncertain significance |
| rs943712164 | 10:126,172,796 | G/C | — | uncertain significance |
| rs1331086977 | 10:126,172,886 | A/T | — | uncertain significance |
| rs112299803 | 10:126,172,901 | A/C | — | likely benign |
| rs545292447 | 10:126,172,954 | G/A | — | — |
| rs761368235 | 10:126,176,997 | G/A | — | uncertain significance |
| rs2494775050 | 10:126,177,045 | T/C | — | uncertain significance |
| rs200710743 | 10:126,177,053 | G/A | — | uncertain significance |
| rs1469055737 | 10:126,177,089 | G/A | — | uncertain significance |
| rs773987254 | 10:126,177,104 | A/G | — | uncertain significance |
| rs777259817 | 10:126,177,137 | G/A | — | uncertain significance |
| rs567294260 | 10:126,178,340 | T/A | — | — |
| rs535437280 | 10:126,182,620 | C/T | — | — |
| rs199754897 | 10:126,185,531 | C/T | — | uncertain significance |
| rs2494829147 | 10:126,185,561 | C/G | — | uncertain significance |
| rs375457352 | 10:126,186,641 | C/A | — | uncertain significance |
| rs376072502 | 10:126,186,647 | C/T | — | uncertain significance |
| rs763505137 | 10:126,205,752 | G/A | — | likely benign |
| rs140823928 | 10:126,205,767 | G/A | — | benign |
| rs538187592 | 10:126,205,785 | G/A | — | uncertain significance |
| rs201727503 | 10:126,205,797 | C/T | — | uncertain significance |
| rs573011028 | 10:126,205,816 | T/G | — | uncertain significance |
| rs61738754 | 10:126,205,829 | C/T | — | benign |
| rs188738583 | 10:126,223,051 | G/A | regulatory region variant | — |
| rs112229674 | 10:126,242,184 | C/G | intron variant | — |
| rs35936514 | 10:126,244,970 | C/T | intron variant | — |
| rs10901769 | 10:126,264,311 | G/A | — | — |
| rs12773846 | 10:126,275,914 | G/C | — | — |
| rs2362501 | 10:126,290,498 | G/A | intron variant | — |
| rs3740540 | 10:126,294,167 | G/A | intron variant | — |
| rs12246623 | 10:126,294,395 | A/G | — | — |
| rs528474716 | 10:126,301,843 | G/A | — | uncertain significance |
| rs376798947 | 10:126,301,853 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.