LRRC32
leucine rich repeat containing 32
Summary
This gene encodes a type I membrane protein which contains 20 leucine-rich repeats. Alterations in the chromosomal region 11q13-11q14 are involved in several pathologies. [provided by RefSeq, Jul 2008]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7685 | 11:76,368,639 | A/C | upstream gene variant | — |
| rs149032268 | 11:76,369,022 | A/G | — | benign |
| rs146793058 | 11:76,370,661 | T/G | — | uncertain significance |
| rs200893333 | 11:76,370,679 | C/T | — | uncertain significance |
| rs200290754 | 11:76,370,857 | C/T | — | uncertain significance |
| rs754675008 | 11:76,370,863 | C/T | — | uncertain significance |
| rs565593386 | 11:76,370,871 | C/T | — | uncertain significance |
| rs202216778 | 11:76,370,909 | G/A | — | likely benign |
| rs137916255 | 11:76,370,918 | G/A | — | likely benign |
| rs371873348 | 11:76,370,946 | C/T | — | uncertain significance |
| rs369867819 | 11:76,371,007 | G/A | — | pathogenic |
| rs200260908 | 11:76,371,046 | C/A | — | uncertain significance |
| rs149468815 | 11:76,371,070 | C/T | — | uncertain significance |
| rs750756039 | 11:76,371,078 | T/C | — | uncertain significance |
| rs2495722464 | 11:76,371,082 | G/A | — | uncertain significance |
| rs115658755 | 11:76,371,084 | C/T | — | likely benign |
| rs749871861 | 11:76,371,086 | C/A | — | uncertain significance |
| rs764702699 | 11:76,371,123 | A/T | — | uncertain significance |
| rs775013615 | 11:76,371,125 | C/A | — | uncertain significance |
| rs762398065 | 11:76,371,127 | T/C | — | uncertain significance |
| rs140060272 | 11:76,371,133 | C/T | — | uncertain significance |
| rs766920653 | 11:76,371,139 | C/T | — | uncertain significance |
| rs779587215 | 11:76,371,165 | G/A | — | uncertain significance |
| rs373530634 | 11:76,371,181 | A/G | — | likely benign |
| rs745681566 | 11:76,371,189 | G/A | — | uncertain significance |
| rs2495723437 | 11:76,371,207 | G/A | — | uncertain significance |
| rs141756735 | 11:76,371,228 | T/C | — | uncertain significance |
| rs202023824 | 11:76,371,252 | G/A | — | uncertain significance |
| rs150588636 | 11:76,371,259 | C/A | — | likely benign |
| rs145077681 | 11:76,371,300 | C/A | — | uncertain significance |
| rs200264908 | 11:76,371,317 | G/A | — | benign |
| rs373117755 | 11:76,371,333 | C/T | — | uncertain significance |
| rs764680966 | 11:76,371,334 | C/T | — | likely benign |
| rs111673552 | 11:76,371,361 | C/G | — | uncertain significance |
| rs573687575 | 11:76,371,396 | C/T | — | uncertain significance |
| rs774839334 | 11:76,371,442 | G/A | — | uncertain significance |
| rs138665218 | 11:76,371,446 | G/A | — | likely benign |
| rs748881614 | 11:76,371,468 | G/A | — | uncertain significance |
| rs754104595 | 11:76,371,471 | C/T | — | uncertain significance |
| rs150096749 | 11:76,371,565 | G/A | — | uncertain significance |
| rs201222193 | 11:76,371,568 | G/A | — | uncertain significance |
| rs571996237 | 11:76,371,582 | C/T | — | uncertain significance |
| rs2495726825 | 11:76,371,639 | C/T | — | uncertain significance |
| rs2120049760 | 11:76,371,657 | A/G | — | likely pathogenic |
| rs867566 | 11:76,371,677 | C/T | — | likely benign |
| rs761862218 | 11:76,371,706 | C/T | — | uncertain significance |
| rs201402758 | 11:76,371,849 | G/C | — | uncertain significance |
| rs150621370 | 11:76,371,886 | G/A | — | uncertain significance |
| rs769250418 | 11:76,371,895 | G/C | — | uncertain significance |
| rs867329262 | 11:76,371,982 | G/C | — | uncertain significance |
| rs2495730238 | 11:76,372,012 | G/T | — | uncertain significance |
| rs369287185 | 11:76,372,045 | G/A | — | likely benign |
| rs144938321 | 11:76,372,058 | G/A | — | likely benign |
| rs34672185 | 11:76,372,064 | G/A | — | likely benign |
| rs747843760 | 11:76,372,067 | A/T | — | uncertain significance |
| rs1400116616 | 11:76,372,095 | T/C | — | uncertain significance |
| rs1471143455 | 11:76,372,140 | C/T | — | uncertain significance |
| rs778615571 | 11:76,372,141 | G/A | — | uncertain significance |
| rs369688581 | 11:76,372,210 | G/A | — | uncertain significance |
| rs1198333582 | 11:76,372,233 | C/T | — | uncertain significance |
| rs756889882 | 11:76,372,261 | C/T | — | uncertain significance |
| rs140733002 | 11:76,372,263 | C/T | — | benign |
| rs201131944 | 11:76,372,296 | G/A | — | uncertain significance |
| rs763968734 | 11:76,372,303 | C/T | — | uncertain significance |
| rs980832833 | 11:76,372,315 | G/A | — | uncertain significance |
| rs1952528641 | 11:76,372,388 | A/C | — | uncertain significance |
| rs771572974 | 11:76,372,493 | C/T | — | likely benign |
| rs745971810 | 11:76,372,503 | G/A | — | likely benign |
| rs374812466 | 11:76,372,525 | G/T | — | uncertain significance |
| rs1251757869 | 11:76,376,901 | G/T | — | likely pathogenic |
| rs147425808 | 11:76,376,970 | G/T | — | uncertain significance |
| rs147482218 | 11:76,378,686 | T/G | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.