PLEKHA6
pleckstrin homology domain containing A6
Known Variants100 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12401452 | 1:204,188,459 | G/A | 3 prime UTR variant | — |
| rs2527608931 | 1:204,192,611 | G/T | — | uncertain significance |
| rs1282276889 | 1:204,192,629 | C/T | — | uncertain significance |
| rs145148095 | 1:204,192,659 | G/A | — | likely benign |
| rs138032109 | 1:204,197,220 | T/G | — | uncertain significance |
| rs761758129 | 1:204,197,253 | C/T | — | uncertain significance |
| rs200309057 | 1:204,197,313 | C/T | — | uncertain significance |
| rs376064147 | 1:204,197,336 | A/G | — | uncertain significance |
| rs747730684 | 1:204,197,943 | A/G | — | uncertain significance |
| rs148649544 | 1:204,197,956 | G/A | — | uncertain significance |
| rs763078149 | 1:204,197,985 | G/A | — | uncertain significance |
| rs145574759 | 1:204,198,100 | C/G | — | uncertain significance |
| rs138582496 | 1:204,198,120 | C/T | — | uncertain significance |
| rs759911278 | 1:204,198,121 | G/A | — | uncertain significance |
| rs751281668 | 1:204,198,135 | C/T | — | uncertain significance |
| rs773428693 | 1:204,198,153 | T/C | — | uncertain significance |
| rs372056044 | 1:204,198,157 | C/T | — | uncertain significance |
| rs749169337 | 1:204,198,219 | C/T | — | uncertain significance |
| rs147239771 | 1:204,198,228 | C/T | — | uncertain significance |
| rs774866824 | 1:204,199,557 | C/T | — | uncertain significance |
| rs369392643 | 1:204,199,561 | G/C | — | likely benign |
| rs780205549 | 1:204,199,605 | C/T | — | uncertain significance |
| rs146418097 | 1:204,199,606 | G/A | — | uncertain significance |
| rs373770957 | 1:204,199,639 | G/A | — | uncertain significance |
| rs4951322 | 1:204,206,270 | G/C | intron variant | — |
| rs998089489 | 1:204,210,528 | C/T | — | uncertain significance |
| rs2527959764 | 1:204,210,569 | A/T | — | likely benign |
| rs146451585 | 1:204,210,600 | A/G | — | uncertain significance |
| rs61755452 | 1:204,210,604 | C/T | — | likely benign |
| rs1379096807 | 1:204,210,872 | A/T | — | uncertain significance |
| rs774563127 | 1:204,213,994 | C/T | — | uncertain significance |
| rs777129079 | 1:204,214,047 | G/A | — | uncertain significance |
| rs535032001 | 1:204,214,757 | G/A | — | uncertain significance |
| rs374244431 | 1:204,214,769 | C/T | — | uncertain significance |
| rs377093823 | 1:204,214,770 | G/A | — | uncertain significance |
| rs1663558507 | 1:204,214,815 | T/C | — | uncertain significance |
| rs773717530 | 1:204,214,838 | C/T | — | uncertain significance |
| rs201432117 | 1:204,216,497 | G/A | — | likely benign |
| rs185597768 | 1:204,216,581 | G/C | — | uncertain significance |
| rs746710062 | 1:204,216,588 | C/T | — | uncertain significance |
| rs201509011 | 1:204,217,950 | G/A | — | uncertain significance |
| rs1345456251 | 1:204,218,035 | C/T | — | uncertain significance |
| rs970345344 | 1:204,218,322 | C/T | — | uncertain significance |
| rs762186576 | 1:204,218,341 | G/A | — | uncertain significance |
| rs766348547 | 1:204,226,492 | T/C | — | uncertain significance |
| rs749809491 | 1:204,226,545 | C/T | — | uncertain significance |
| rs367949377 | 1:204,226,546 | G/A | — | uncertain significance |
| rs538673591 | 1:204,226,549 | G/A | — | uncertain significance |
| rs770691409 | 1:204,226,572 | C/G | — | uncertain significance |
| rs769675445 | 1:204,226,582 | G/A | — | uncertain significance |
| rs752263935 | 1:204,226,633 | G/A | — | uncertain significance |
| rs190536669 | 1:204,226,668 | C/T | — | uncertain significance |
| rs762871642 | 1:204,226,671 | C/T | — | uncertain significance |
| rs760840127 | 1:204,226,680 | C/T | — | uncertain significance |
| rs375139317 | 1:204,226,687 | C/T | — | uncertain significance |
| rs1485725746 | 1:204,226,711 | C/A | — | uncertain significance |
| rs771067288 | 1:204,226,756 | G/A | — | uncertain significance |
| rs766305489 | 1:204,226,768 | C/G | — | uncertain significance |
| rs145170381 | 1:204,226,803 | C/A | — | uncertain significance |
| rs527810742 | 1:204,226,807 | C/T | — | uncertain significance |
| rs369190008 | 1:204,226,816 | G/A | — | uncertain significance |
| rs138411516 | 1:204,226,851 | G/A | — | uncertain significance |
| rs754872740 | 1:204,226,872 | G/A | — | uncertain significance |
| rs148442755 | 1:204,226,917 | T/C | — | uncertain significance |
| rs745311178 | 1:204,228,390 | G/A | — | uncertain significance |
| rs2527431369 | 1:204,228,414 | C/T | — | uncertain significance |
| rs1157499639 | 1:204,228,417 | G/A | — | uncertain significance |
| rs768382723 | 1:204,228,476 | T/C | — | uncertain significance |
| rs201176357 | 1:204,228,503 | C/T | — | uncertain significance |
| rs779459555 | 1:204,228,530 | T/G | — | uncertain significance |
| rs147420132 | 1:204,228,558 | G/A | — | uncertain significance |
| rs1298294292 | 1:204,228,566 | G/A | — | uncertain significance |
| rs149502738 | 1:204,228,587 | G/A | — | uncertain significance |
| rs377234378 | 1:204,228,600 | G/C | — | uncertain significance |
| rs2527441937 | 1:204,228,633 | G/A | — | uncertain significance |
| rs777454219 | 1:204,228,647 | G/A | — | uncertain significance |
| rs750766785 | 1:204,228,690 | T/C | — | uncertain significance |
| rs1259853839 | 1:204,228,813 | G/T | — | uncertain significance |
| rs201770834 | 1:204,228,828 | G/C | — | uncertain significance |
| rs2527496726 | 1:204,230,497 | C/T | — | uncertain significance |
| rs775381290 | 1:204,234,077 | G/A | — | uncertain significance |
| rs750532561 | 1:204,234,087 | G/A | — | uncertain significance |
| rs776577342 | 1:204,236,618 | G/C | — | uncertain significance |
| rs1196925697 | 1:204,236,623 | C/A | — | uncertain significance |
| rs200274685 | 1:204,236,624 | G/A | — | uncertain significance |
| rs150307846 | 1:204,237,355 | G/A | — | uncertain significance |
| rs199871600 | 1:204,237,368 | G/T | — | uncertain significance |
| rs2527661302 | 1:204,237,370 | G/A | — | uncertain significance |
| rs145088130 | 1:204,237,434 | G/A | — | uncertain significance |
| rs139666400 | 1:204,237,439 | G/T | — | uncertain significance |
| rs2527664090 | 1:204,237,440 | C/T | — | uncertain significance |
| rs144821028 | 1:204,242,756 | G/A | — | uncertain significance |
| rs4548504 | 1:204,254,762 | C/T | intron variant | — |
| rs16853237 | 1:204,262,260 | T/G | — | — |
| rs6673447 | 1:204,264,542 | C/T | intron variant | — |
| rs35457431 | 1:204,266,749 | G/A | intron variant | — |
| rs7534537 | 1:204,274,519 | T/C | intron variant | — |
| rs4245729 | 1:204,289,393 | G/A | regulatory region variant | — |
| rs7513240 | 1:204,319,907 | C/G | — | — |
| rs10793761 | 1:204,321,018 | A/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.