LYPD3
LY6/PLAUR domain containing 3
Summary
Predicted to enable laminin binding activity. Involved in negative regulation of smooth muscle cell apoptotic process. Located in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs34034481 | 19:43,965,527 | G/A | — | benign |
| rs965834420 | 19:43,965,538 | G/A | — | uncertain significance |
| rs2513515753 | 19:43,965,546 | A/G | — | uncertain significance |
| rs149095976 | 19:43,965,594 | C/T | missense variant | — |
| rs554745791 | 19:43,965,646 | C/T | — | uncertain significance |
| rs1251326118 | 19:43,965,670 | C/T | — | uncertain significance |
| rs746415612 | 19:43,965,676 | G/A | — | uncertain significance |
| rs1191866950 | 19:43,965,729 | A/G | — | likely benign |
| rs28477226 | 19:43,965,804 | G/T | — | benign |
| rs1568467173 | 19:43,965,876 | G/C | — | uncertain significance |
| rs767515075 | 19:43,965,886 | G/A | — | uncertain significance |
| rs150547456 | 19:43,965,915 | G/A | — | uncertain significance |
| rs764206499 | 19:43,965,964 | C/T | — | uncertain significance |
| rs1970778901 | 19:43,965,978 | G/A | — | uncertain significance |
| rs2682581 | 19:43,966,506 | C/G | intron variant | — |
| rs199756903 | 19:43,967,813 | T/C | — | uncertain significance |
| rs779567306 | 19:43,967,920 | G/C | — | uncertain significance |
| rs754981572 | 19:43,968,521 | G/A | — | uncertain significance |
| rs1352225163 | 19:43,968,534 | C/T | — | uncertain significance |
| rs772588419 | 19:43,968,561 | C/T | — | uncertain significance |
| rs752733095 | 19:43,968,606 | C/T | — | uncertain significance |
| rs147118068 | 19:43,969,667 | C/T | — | benign |
| rs200130720 | 19:43,969,713 | G/A | — | uncertain significance |
| rs755517527 | 19:43,969,718 | G/C | — | uncertain significance |
| rs3848565 | 19:43,969,840 | G/T | regulatory region variant | — |
| rs187436577 | 19:43,970,891 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.