LY9
lymphocyte antigen 9
Summary
LY9 belongs to the SLAM family of immunomodulatory receptors (see SLAMF1; MIM 603492) and interacts with the adaptor molecule SAP (SH2D1A; MIM 300490) (Graham et al., 2006 [PubMed 16365421]).[supplied by OMIM, Mar 2008]
Known Variants65 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6659569 | 1:160,764,566 | T/C | upstream gene variant | — |
| rs149416710 | 1:160,766,016 | T/C | — | likely benign |
| rs2525372831 | 1:160,766,075 | A/C | — | uncertain significance |
| rs763695887 | 1:160,766,091 | C/G | — | uncertain significance |
| rs975285644 | 1:160,769,569 | G/A | — | uncertain significance |
| rs375226732 | 1:160,769,591 | T/C | — | uncertain significance |
| rs140774383 | 1:160,769,636 | C/T | — | uncertain significance |
| rs1318612242 | 1:160,769,687 | C/T | — | uncertain significance |
| rs200948203 | 1:160,769,689 | C/T | — | uncertain significance |
| rs35759983 | 1:160,769,690 | G/A | — | likely benign |
| rs748971556 | 1:160,769,700 | A/C | — | uncertain significance |
| rs768514092 | 1:160,769,708 | C/A | — | uncertain significance |
| rs146162790 | 1:160,769,768 | G/A | — | uncertain significance |
| rs474918 | 1:160,771,197 | C/G | — | — |
| rs1556517 | 1:160,771,761 | C/T | — | — |
| rs114278810 | 1:160,774,690 | C/T | intron variant | — |
| rs181763581 | 1:160,778,894 | C/T | intron variant | — |
| rs541794161 | 1:160,780,366 | G/A | — | — |
| rs4656933 | 1:160,782,561 | T/C | — | — |
| rs41266929 | 1:160,783,223 | C/G | regulatory region variant | — |
| rs189330177 | 1:160,783,435 | A/G | — | uncertain significance |
| rs1233609638 | 1:160,783,502 | G/A | — | uncertain significance |
| rs1313699841 | 1:160,783,506 | T/G | — | uncertain significance |
| rs376341054 | 1:160,783,515 | G/A | — | uncertain significance |
| rs1010716482 | 1:160,783,528 | G/C | — | uncertain significance |
| rs35923801 | 1:160,783,557 | A/C | — | benign |
| rs200190832 | 1:160,783,678 | T/C | — | uncertain significance |
| rs769390084 | 1:160,784,251 | G/T | — | uncertain significance |
| rs148338202 | 1:160,784,303 | G/A | — | likely benign |
| rs3737783 | 1:160,784,320 | G/A | — | uncertain significance |
| rs751324638 | 1:160,784,356 | A/G | — | uncertain significance |
| rs139473900 | 1:160,784,398 | G/C | — | uncertain significance |
| rs571520073 | 1:160,786,408 | C/T | — | uncertain significance |
| rs747172463 | 1:160,786,414 | G/T | — | uncertain significance |
| rs776247637 | 1:160,786,416 | C/T | — | uncertain significance |
| rs773175503 | 1:160,786,432 | A/T | — | uncertain significance |
| rs377674002 | 1:160,786,473 | G/A | — | uncertain significance |
| rs750912918 | 1:160,786,480 | A/T | — | uncertain significance |
| rs2525550699 | 1:160,786,538 | A/C | — | uncertain significance |
| rs199688790 | 1:160,786,621 | C/G | — | uncertain significance |
| rs751688961 | 1:160,786,632 | C/A | — | uncertain significance |
| rs114914487 | 1:160,787,303 | A/G | intron variant | — |
| rs181984842 | 1:160,787,695 | G/A | intron variant | — |
| rs201049859 | 1:160,788,068 | T/C | — | uncertain significance |
| rs145664274 | 1:160,788,097 | C/T | — | likely benign |
| rs565586848 | 1:160,788,239 | G/T | — | — |
| rs2525574245 | 1:160,789,128 | T/C | — | uncertain significance |
| rs768884657 | 1:160,789,153 | C/T | — | uncertain significance |
| rs2027015 | 1:160,791,778 | G/A | regulatory region variant | — |
| rs494091 | 1:160,791,892 | T/A | — | — |
| rs2525612181 | 1:160,793,317 | C/A | — | uncertain significance |
| rs1021219176 | 1:160,793,327 | C/T | — | uncertain significance |
| rs748609074 | 1:160,793,426 | G/A | — | likely benign |
| rs146895414 | 1:160,793,445 | T/A | — | uncertain significance |
| rs1223582573 | 1:160,793,468 | C/G | — | uncertain significance |
| rs2525614024 | 1:160,793,470 | G/A | — | uncertain significance |
| rs509749 | 1:160,793,560 | A/G | missense variant | benign |
| rs763258613 | 1:160,793,561 | T/C | — | uncertain significance |
| rs761006278 | 1:160,794,000 | G/C | — | uncertain significance |
| rs556810 | 1:160,794,456 | A/G | intron variant | — |
| rs504848 | 1:160,794,497 | C/T | intron variant | — |
| rs144930893 | 1:160,796,941 | C/A | downstream gene variant | — |
| rs576334 | 1:160,797,514 | C/G | regulatory region variant | — |
| rs775115570 | 1:160,797,553 | C/G | — | uncertain significance |
| rs569911 | 1:160,798,209 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.