LRIT2
leucine rich repeat, Ig-like and transmembrane domains 2
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139824036 | 10:85,980,992 | T/G | downstream gene variant | — |
| rs753366582 | 10:85,981,696 | C/T | — | uncertain significance |
| rs570085431 | 10:85,981,725 | A/G | — | uncertain significance |
| rs6585847 | 10:85,981,801 | T/G | — | uncertain significance |
| rs143323013 | 10:85,981,812 | G/C | — | uncertain significance |
| rs147546091 | 10:85,981,821 | C/T | — | uncertain significance |
| rs766565567 | 10:85,981,836 | C/T | — | uncertain significance |
| rs372043491 | 10:85,981,837 | G/A | — | likely benign |
| rs190259697 | 10:85,981,867 | C/T | — | uncertain significance |
| rs747387009 | 10:85,981,888 | C/T | — | uncertain significance |
| rs781380404 | 10:85,981,890 | C/T | — | uncertain significance |
| rs1405621901 | 10:85,981,957 | C/G | — | uncertain significance |
| rs767848046 | 10:85,982,062 | G/A | — | uncertain significance |
| rs200602947 | 10:85,982,149 | A/T | — | uncertain significance |
| rs746969088 | 10:85,982,166 | G/A | — | uncertain significance |
| rs1842519437 | 10:85,982,173 | C/A | — | uncertain significance |
| rs147451139 | 10:85,982,223 | C/T | — | uncertain significance |
| rs369686448 | 10:85,982,343 | G/C | — | uncertain significance |
| rs780261945 | 10:85,982,344 | C/A | — | uncertain significance |
| rs376534012 | 10:85,982,394 | A/G | — | uncertain significance |
| rs768254427 | 10:85,984,116 | G/T | — | uncertain significance |
| rs2492586735 | 10:85,984,178 | T/A | — | uncertain significance |
| rs2492586918 | 10:85,984,223 | G/T | — | uncertain significance |
| rs149117326 | 10:85,984,260 | G/C | — | uncertain significance |
| rs368450994 | 10:85,984,266 | C/T | — | uncertain significance |
| rs199677093 | 10:85,984,439 | C/T | — | likely benign |
| rs767828408 | 10:85,984,455 | C/T | — | uncertain significance |
| rs368409346 | 10:85,984,512 | C/A | — | uncertain significance |
| rs1842546550 | 10:85,984,534 | G/T | — | uncertain significance |
| rs533863666 | 10:85,984,595 | A/G | — | uncertain significance |
| rs138269963 | 10:85,984,601 | G/C | — | uncertain significance |
| rs780942855 | 10:85,984,605 | T/C | — | uncertain significance |
| rs369090928 | 10:85,984,616 | G/A | — | uncertain significance |
| rs369752604 | 10:85,984,688 | G/A | — | uncertain significance |
| rs373533928 | 10:85,984,748 | A/G | — | uncertain significance |
| rs139238795 | 10:85,985,183 | C/T | — | uncertain significance |
| rs369307601 | 10:85,985,216 | G/C | — | uncertain significance |
| rs745480 | 10:85,986,554 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.