LY75
lymphocyte antigen 75
Summary
Predicted to enable signaling receptor activity. Predicted to be involved in immune response and inflammatory response. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs72965376 | 2:160,659,737 | A/T | upstream gene variant | — |
| rs746382082 | 2:160,661,582 | C/G | — | uncertain significance |
| rs768824949 | 2:160,661,604 | G/A | — | uncertain significance |
| rs34034503 | 2:160,661,610 | C/G | — | conflicting classifications of pathogenicity |
| rs770091214 | 2:160,661,672 | G/A | — | likely benign |
| rs1549577 | 2:160,665,278 | C/T | downstream gene variant | — |
| rs186728746 | 2:160,673,630 | G/A | upstream gene variant | — |
| rs62175230 | 2:160,677,674 | C/G | — | — |
| rs60264981 | 2:160,677,998 | T/C | — | — |
| rs147296947 | 2:160,678,349 | G/A | intron variant | — |
| rs12053269 | 2:160,679,238 | T/G | intron variant | — |
| rs62175254 | 2:160,682,108 | C/G | — | — |
| rs2955982 | 2:160,683,524 | G/C | — | — |
| rs2729703 | 2:160,684,654 | C/A | — | — |
| rs2729707 | 2:160,687,231 | A/T | — | — |
| rs113023766 | 2:160,688,217 | T/C | missense variant | — |
| rs6755783 | 2:160,688,351 | C/T | intron variant | — |
| rs188074213 | 2:160,689,335 | G/A | intron variant | — |
| rs141059884 | 2:160,691,838 | T/C | intron variant | — |
| rs140695949 | 2:160,692,117 | G/A | — | likely benign |
| rs181965570 | 2:160,692,773 | G/A | intron variant | — |
| rs11896565 | 2:160,696,242 | C/G | — | — |
| rs78685880 | 2:160,706,544 | A/G | missense variant | — |
| rs149297961 | 2:160,706,931 | G/T | — | likely benign |
| rs146290413 | 2:160,711,364 | T/C | intron variant | — |
| rs138319240 | 2:160,711,454 | T/C | — | benign |
| rs114821641 | 2:160,714,958 | C/T | stop gained | — |
| rs72955755 | 2:160,718,332 | C/G | intron variant | — |
| rs7564243 | 2:160,726,868 | G/T | — | — |
| rs34020639 | 2:160,729,082 | A/G | — | benign |
| rs116474493 | 2:160,732,144 | G/A | — | benign |
| rs187326737 | 2:160,732,372 | G/A | intron variant | — |
| rs148976305 | 2:160,732,572 | C/T | intron variant | — |
| rs545499741 | 2:160,734,874 | G/A | — | uncertain significance |
| rs115254354 | 2:160,735,190 | C/A | — | benign |
| rs114727644 | 2:160,735,191 | C/A | — | benign |
| rs77761086 | 2:160,735,775 | C/T | — | benign |
| rs114320498 | 2:160,735,802 | C/T | — | likely benign |
| rs79199281 | 2:160,737,717 | G/A | — | benign |
| rs35675007 | 2:160,738,803 | G/A | — | benign |
| rs146598746 | 2:160,740,694 | C/T | intron variant | — |
| rs28378710 | 2:160,744,092 | A/G | intron variant | — |
| rs186286806 | 2:160,747,504 | C/T | regulatory region variant | — |
| rs559880111 | 2:160,754,487 | A/C | — | — |
| rs150493510 | 2:160,755,340 | T/G | — | uncertain significance |
| rs149458354 | 2:160,755,351 | A/G | — | uncertain significance |
| rs1397707 | 2:160,760,972 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.