LRCH3
leucine rich repeats and calponin homology domain containing 3
Summary
Involved in septin cytoskeleton organization. Located in cytosol. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants66 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374623656 | 3:197,518,140 | C/T | — | likely benign |
| rs146048989 | 3:197,518,155 | G/A | — | likely benign |
| rs143455842 | 3:197,518,173 | T/C | — | likely benign |
| rs746914318 | 3:197,518,216 | G/A | — | uncertain significance |
| rs979092708 | 3:197,518,228 | G/A | — | uncertain significance |
| rs371288838 | 3:197,518,235 | A/C | — | uncertain significance |
| rs762539091 | 3:197,518,256 | C/A | — | uncertain significance |
| rs778870012 | 3:197,518,276 | G/T | — | uncertain significance |
| rs781213558 | 3:197,518,303 | G/T | — | uncertain significance |
| rs368207979 | 3:197,518,348 | C/T | — | uncertain significance |
| rs750518494 | 3:197,518,366 | C/T | — | uncertain significance |
| rs1730493375 | 3:197,518,373 | G/A | — | uncertain significance |
| rs756042466 | 3:197,518,405 | C/T | — | uncertain significance |
| rs376192844 | 3:197,541,776 | T/C | — | likely benign |
| rs201645357 | 3:197,541,796 | C/T | — | uncertain significance |
| rs150956786 | 3:197,544,082 | G/A | — | likely benign |
| rs375478596 | 3:197,544,115 | A/G | — | uncertain significance |
| rs752398902 | 3:197,544,145 | T/C | — | uncertain significance |
| rs1733910370 | 3:197,544,147 | G/C | — | uncertain significance |
| rs746335994 | 3:197,544,160 | A/G | — | uncertain significance |
| rs1280579941 | 3:197,547,281 | A/C | — | uncertain significance |
| rs371394845 | 3:197,553,758 | A/G | — | uncertain significance |
| rs571932314 | 3:197,553,770 | T/A | — | uncertain significance |
| rs1410759981 | 3:197,553,842 | C/T | — | likely benign |
| rs371931398 | 3:197,556,484 | C/T | — | uncertain significance |
| rs35040867 | 3:197,556,508 | C/T | — | uncertain significance |
| rs148382632 | 3:197,556,527 | G/A | — | likely benign |
| rs501101 | 3:197,557,635 | C/T | — | benign |
| rs781649324 | 3:197,557,663 | C/T | — | uncertain significance |
| rs773418585 | 3:197,557,694 | A/G | — | uncertain significance |
| rs143788297 | 3:197,559,073 | A/G | — | likely benign |
| rs765987791 | 3:197,559,098 | C/G | — | uncertain significance |
| rs2529688568 | 3:197,559,122 | C/G | — | uncertain significance |
| rs185178446 | 3:197,559,141 | G/T | — | uncertain significance |
| rs201329913 | 3:197,559,159 | G/A | — | uncertain significance |
| rs374224629 | 3:197,562,589 | G/A | — | uncertain significance |
| rs1736698066 | 3:197,562,594 | G/C | — | uncertain significance |
| rs368401680 | 3:197,562,607 | G/A | — | uncertain significance |
| rs1174866875 | 3:197,562,642 | C/A | — | uncertain significance |
| rs571384152 | 3:197,562,680 | G/T | — | uncertain significance |
| rs1043169943 | 3:197,566,188 | C/T | — | likely benign |
| rs375044345 | 3:197,566,206 | G/C | — | uncertain significance |
| rs148665137 | 3:197,566,233 | A/C | — | likely benign |
| rs144275631 | 3:197,566,250 | G/A | — | uncertain significance |
| rs17850206 | 3:197,566,254 | C/T | — | benign |
| rs1738996067 | 3:197,574,797 | A/T | — | uncertain significance |
| rs35713063 | 3:197,574,881 | G/A | — | uncertain significance |
| rs1739754028 | 3:197,579,447 | A/G | — | uncertain significance |
| rs36078463 | 3:197,579,466 | T/C | — | benign |
| rs1250564577 | 3:197,581,299 | G/T | — | uncertain significance |
| rs778617574 | 3:197,585,707 | G/A | — | likely benign |
| rs747828697 | 3:197,592,998 | C/T | — | uncertain significance |
| rs762169755 | 3:197,593,037 | A/T | — | uncertain significance |
| rs761935258 | 3:197,593,041 | C/T | — | likely benign |
| rs141489799 | 3:197,597,033 | C/T | — | uncertain significance |
| rs77281724 | 3:197,597,044 | C/T | — | benign |
| rs2530022168 | 3:197,597,088 | T/G | — | uncertain significance |
| rs775990454 | 3:197,597,135 | G/A | — | uncertain significance |
| rs141761986 | 3:197,597,144 | C/T | — | likely benign |
| rs371803335 | 3:197,597,145 | G/A | — | uncertain significance |
| rs1481276099 | 3:197,598,223 | C/G | — | uncertain significance |
| rs774064523 | 3:197,598,278 | C/T | — | uncertain significance |
| rs73089368 | 3:197,598,307 | A/G | — | uncertain significance |
| rs2530055344 | 3:197,602,582 | T/C | — | uncertain significance |
| rs1346288310 | 3:197,607,490 | C/G | — | likely benign |
| rs186865549 | 3:197,610,974 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.