LRRC37A2
leucine rich repeat containing 37 member A2
Summary
Predicted to enable ATP binding activity; ATP hydrolysis activity; and metal ion binding activity. Predicted to be involved in SNARE complex disassembly and protein transport. Predicted to be located in cytoplasm and membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants87 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs554105021 | 17:44,482,352 | T/G | — | — |
| rs1244020901 | 17:44,487,793 | G/C | — | — |
| rs545131906 | 17:44,497,879 | G/C | — | — |
| rs1191835359 | 17:44,515,243 | C/T | — | — |
| rs369136006 | 17:44,517,763 | A/T | — | — |
| rs557236423 | 17:44,517,766 | T/A | — | — |
| rs155779 | 17:44,521,740 | G/A | — | — |
| rs75104997 | 17:44,573,874 | C/A | — | — |
| rs2942003 | 17:44,576,704 | T/C | — | — |
| rs1333353619 | 17:44,590,107 | T/C | — | likely benign |
| rs1239468440 | 17:44,590,128 | G/A | — | uncertain significance |
| rs1319456896 | 17:44,590,175 | C/G | — | uncertain significance |
| rs373973615 | 17:44,590,283 | C/T | — | likely benign |
| rs544698022 | 17:44,590,338 | T/C | — | uncertain significance |
| rs1211689881 | 17:44,590,383 | C/T | — | likely benign |
| rs1467971487 | 17:44,590,401 | C/A | — | uncertain significance |
| rs1249441311 | 17:44,590,526 | C/G | — | uncertain significance |
| rs1245972263 | 17:44,590,674 | T/G | — | uncertain significance |
| rs1280064300 | 17:44,590,677 | G/A | — | uncertain significance |
| rs1195171075 | 17:44,590,788 | C/T | — | likely benign |
| rs2051093478 | 17:44,590,818 | C/T | — | uncertain significance |
| rs775920840 | 17:44,592,057 | G/A | — | likely benign |
| rs755924095 | 17:44,592,315 | C/T | — | uncertain significance |
| rs1329285196 | 17:44,592,353 | C/T | — | uncertain significance |
| rs199621736 | 17:44,592,405 | G/A | — | likely benign |
| rs550252059 | 17:44,592,407 | C/A | — | uncertain significance |
| rs1397191052 | 17:44,592,544 | C/G | — | likely benign |
| rs1163124862 | 17:44,594,794 | G/C | — | uncertain significance |
| rs997023164 | 17:44,618,222 | A/G | — | uncertain significance |
| rs768540224 | 17:44,623,640 | G/A | — | uncertain significance |
| rs774129178 | 17:44,623,658 | T/C | — | uncertain significance |
| rs1416499803 | 17:44,625,747 | C/T | — | uncertain significance |
| rs751952249 | 17:44,625,842 | G/A | — | uncertain significance |
| rs2545615752 | 17:44,625,945 | C/T | — | uncertain significance |
| rs1567979523 | 17:44,625,951 | A/G | — | uncertain significance |
| rs764584933 | 17:44,625,974 | G/C | — | uncertain significance |
| rs200087533 | 17:44,626,000 | G/T | — | likely benign |
| rs746622571 | 17:44,626,001 | A/G | — | uncertain significance |
| rs753897441 | 17:44,626,042 | C/G | — | uncertain significance |
| rs371330917 | 17:44,626,097 | G/C | — | uncertain significance |
| rs751355590 | 17:44,626,124 | G/A | — | likely benign |
| rs374053039 | 17:44,626,137 | C/T | — | uncertain significance |
| rs2056469278 | 17:44,626,144 | G/C | — | uncertain significance |
| rs779500864 | 17:44,626,145 | G/C | — | likely benign |
| rs1246730710 | 17:44,626,175 | G/A | — | uncertain significance |
| rs553938756 | 17:44,626,217 | A/C | — | uncertain significance |
| rs2056485610 | 17:44,626,233 | C/T | — | uncertain significance |
| rs781778252 | 17:44,626,251 | A/C | — | uncertain significance |
| rs774230393 | 17:44,626,266 | G/A | — | uncertain significance |
| rs542986463 | 17:44,626,274 | T/C | — | uncertain significance |
| rs1431039661 | 17:44,626,296 | C/A | — | uncertain significance |
| rs201311857 | 17:44,626,301 | C/T | — | uncertain significance |
| rs775169826 | 17:44,626,380 | C/T | — | likely benign |
| rs773941851 | 17:44,626,385 | A/G | — | likely benign |
| rs372848109 | 17:44,626,422 | G/A | — | uncertain significance |
| rs764265934 | 17:44,626,458 | C/T | — | uncertain significance |
| rs2056529533 | 17:44,626,467 | T/A | — | uncertain significance |
| rs773349277 | 17:44,626,578 | C/A | — | uncertain significance |
| rs2056575213 | 17:44,626,774 | T/G | — | uncertain significance |
| rs1263990754 | 17:44,626,779 | C/A | — | uncertain significance |
| rs565284869 | 17:44,626,827 | C/G | — | uncertain significance |
| rs758776686 | 17:44,626,853 | G/A | — | likely benign |
| rs1345352872 | 17:44,626,895 | C/T | — | uncertain significance |
| rs1446870318 | 17:44,626,908 | C/G | — | uncertain significance |
| rs374452768 | 17:44,627,853 | A/T | — | uncertain significance |
| rs760524677 | 17:44,627,854 | C/T | — | likely benign |
| rs752772683 | 17:44,630,779 | G/A | — | uncertain significance |
| rs770775064 | 17:44,630,790 | C/G | — | likely benign |
| rs773412579 | 17:44,632,702 | C/T | — | uncertain significance |
| rs780695661 | 17:44,632,746 | C/A | — | uncertain significance |
| rs772152770 | 17:44,632,749 | G/T | — | uncertain significance |
| rs775120595 | 17:44,632,786 | C/A | — | uncertain significance |
| rs762876067 | 17:44,632,789 | G/C | — | uncertain significance |
| rs536035466 | 17:44,632,910 | C/T | — | uncertain significance |
| rs746004658 | 17:44,632,914 | C/T | — | uncertain significance |
| rs1460475747 | 17:44,632,921 | G/T | — | uncertain significance |
| rs545764163 | 17:44,663,783 | C/T | — | — |
| rs199529 | 17:44,837,217 | A/C | downstream gene variant | — |
| rs72836354 | 17:44,899,464 | G/A | regulatory region variant | — |
| rs9890413 | 17:44,901,449 | G/T | — | — |
| rs1221268 | 17:44,903,752 | T/A | — | — |
| rs185884027 | 17:44,980,509 | T/A | intergenic variant | — |
| rs4461138 | 17:44,987,045 | T/G | downstream gene variant | — |
| rs4968247 | 17:44,988,703 | C/A | — | — |
| rs533030436 | 17:45,091,770 | A/G | — | — |
| rs8078336 | 17:45,097,337 | G/T | regulatory region variant | — |
| rs62073767 | 17:45,101,085 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.