LRRC7
leucine rich repeat containing 7
Summary
Predicted to enable protein kinase binding activity. Predicted to be involved in several processes, including establishment or maintenance of epithelial cell apical/basal polarity; positive regulation of neuron projection development; and protein localization to membrane. Located in several cellular components, including centrosome; cytosol; and nucleoplasm. Implicated in cocaine dependence. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants77 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs77668180 | 1:70,060,695 | A/G | — | — |
| rs1418004 | 1:70,117,448 | C/T | intron variant | — |
| rs115352313 | 1:70,144,097 | G/A | — | likely benign |
| rs1417437 | 1:70,154,441 | T/C | intron variant | — |
| rs10889850 | 1:70,207,079 | T/G | intron variant | — |
| rs2523682566 | 1:70,225,948 | G/C | — | uncertain significance |
| rs267598703 | 1:70,257,751 | G/A | — | uncertain significance |
| rs34658389 | 1:70,257,779 | T/C | — | benign |
| rs149282327 | 1:70,267,229 | G/A | intron variant | — |
| rs12026556 | 1:70,282,490 | G/A | intron variant | — |
| rs2524226242 | 1:70,300,477 | T/C | — | uncertain significance |
| rs6691577 | 1:70,302,201 | A/C | — | — |
| rs2226284 | 1:70,335,682 | T/G | — | — |
| rs12037173 | 1:70,355,981 | A/G | intron variant | — |
| rs12756253 | 1:70,396,007 | C/T | intron variant | — |
| rs766970305 | 1:70,397,199 | C/G | — | uncertain significance |
| rs140920935 | 1:70,397,245 | G/A | — | likely benign |
| rs1023008 | 1:70,404,540 | A/G | — | — |
| rs79095525 | 1:70,416,795 | A/G | intron variant | — |
| rs2523321484 | 1:70,452,037 | C/T | — | uncertain significance |
| rs1656539329 | 1:70,477,535 | T/G | — | uncertain significance |
| rs535532334 | 1:70,486,750 | A/G | — | uncertain significance |
| rs201467999 | 1:70,488,818 | T/G | — | uncertain significance |
| rs752772068 | 1:70,488,828 | C/T | — | uncertain significance |
| rs766365842 | 1:70,488,866 | G/T | — | uncertain significance |
| rs201075157 | 1:70,488,881 | G/A | — | uncertain significance |
| rs1657717968 | 1:70,489,019 | G/C | — | uncertain significance |
| rs781712945 | 1:70,489,038 | C/T | — | uncertain significance |
| rs756972138 | 1:70,493,897 | A/G | — | uncertain significance |
| rs200880197 | 1:70,494,035 | C/T | — | uncertain significance |
| rs774424374 | 1:70,501,808 | C/G | — | uncertain significance |
| rs763412623 | 1:70,503,854 | G/T | — | uncertain significance |
| rs1305758247 | 1:70,503,864 | C/T | — | uncertain significance |
| rs1388011161 | 1:70,503,930 | A/G | — | uncertain significance |
| rs769259626 | 1:70,503,936 | C/T | — | uncertain significance |
| rs2523547605 | 1:70,503,999 | C/T | — | uncertain significance |
| rs1246459421 | 1:70,504,032 | C/T | — | uncertain significance |
| rs1182861744 | 1:70,504,040 | C/T | — | uncertain significance |
| rs772544650 | 1:70,504,094 | C/A | — | uncertain significance |
| rs1329735347 | 1:70,504,097 | T/C | — | uncertain significance |
| rs773004438 | 1:70,504,289 | C/T | — | uncertain significance |
| rs780524150 | 1:70,504,367 | C/A | — | uncertain significance |
| rs2523551405 | 1:70,504,460 | T/A | — | uncertain significance |
| rs777857057 | 1:70,504,511 | C/G | — | uncertain significance |
| rs2523552339 | 1:70,504,552 | C/G | — | uncertain significance |
| rs138318831 | 1:70,504,555 | C/A | — | uncertain significance |
| rs371826605 | 1:70,504,556 | G/A | — | uncertain significance |
| rs755491527 | 1:70,504,566 | A/G | — | uncertain significance |
| rs375046296 | 1:70,504,625 | A/G | — | uncertain significance |
| rs2523553327 | 1:70,504,649 | T/C | — | uncertain significance |
| rs981289748 | 1:70,504,650 | A/G | — | uncertain significance |
| rs1558014645 | 1:70,504,653 | G/A | — | uncertain significance |
| rs758326913 | 1:70,504,820 | G/A | — | uncertain significance |
| rs775728075 | 1:70,504,860 | C/T | — | uncertain significance |
| rs377656393 | 1:70,504,863 | C/T | — | uncertain significance |
| rs1659633098 | 1:70,504,871 | C/A | — | uncertain significance |
| rs772640586 | 1:70,504,931 | G/A | — | uncertain significance |
| rs570970804 | 1:70,504,944 | C/T | — | uncertain significance |
| rs748465593 | 1:70,504,983 | G/A | — | uncertain significance |
| rs2523558046 | 1:70,505,054 | A/G | — | uncertain significance |
| rs139513686 | 1:70,505,057 | C/T | — | uncertain significance |
| rs2523558236 | 1:70,505,072 | G/A | — | uncertain significance |
| rs1135401780 | 1:70,505,137 | T/G | — | uncertain significance |
| rs1182565343 | 1:70,505,241 | C/G | — | uncertain significance |
| rs2523560841 | 1:70,505,429 | T/G | — | uncertain significance |
| rs1003227526 | 1:70,509,658 | A/G | — | uncertain significance |
| rs773622605 | 1:70,509,737 | C/T | — | uncertain significance |
| rs776919531 | 1:70,518,766 | G/A | — | uncertain significance |
| rs1339289844 | 1:70,541,760 | G/A | — | uncertain significance |
| rs1024729333 | 1:70,541,814 | C/T | — | uncertain significance |
| rs1376546849 | 1:70,541,827 | C/T | — | uncertain significance |
| rs780581912 | 1:70,541,841 | A/C | — | uncertain significance |
| rs199872098 | 1:70,541,910 | C/T | — | uncertain significance |
| rs573192198 | 1:70,541,911 | G/A | — | uncertain significance |
| rs755373930 | 1:70,541,961 | A/G | — | uncertain significance |
| rs663251 | 1:70,566,021 | G/A | — | — |
| rs2523919523 | 1:70,587,542 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.