PLXDC1
plexin domain containing 1
Summary
Predicted to be involved in angiogenesis. Part of receptor complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761234611 | 17:37,224,151 | G/A | — | uncertain significance |
| rs758450228 | 17:37,224,187 | A/G | — | uncertain significance |
| rs1598180388 | 17:37,224,202 | T/G | — | uncertain significance |
| rs11654947 | 17:37,225,616 | A/G | — | — |
| rs777162271 | 17:37,226,117 | A/G | — | uncertain significance |
| rs752500050 | 17:37,226,183 | C/T | — | uncertain significance |
| rs1233861284 | 17:37,228,708 | C/T | — | uncertain significance |
| rs1437989887 | 17:37,235,368 | A/G | — | uncertain significance |
| rs1375715945 | 17:37,235,392 | G/A | — | uncertain significance |
| rs370370043 | 17:37,235,398 | G/A | — | uncertain significance |
| rs2508726941 | 17:37,239,749 | G/C | — | uncertain significance |
| rs1186101987 | 17:37,239,772 | C/T | — | uncertain significance |
| rs2508757387 | 17:37,243,875 | A/G | — | uncertain significance |
| rs200519422 | 17:37,243,901 | T/C | — | uncertain significance |
| rs139074225 | 17:37,243,938 | T/C | — | uncertain significance |
| rs201383661 | 17:37,243,943 | C/T | — | uncertain significance |
| rs757980543 | 17:37,243,949 | C/T | — | uncertain significance |
| rs377174999 | 17:37,249,883 | C/T | — | — |
| rs775387875 | 17:37,262,136 | A/G | — | uncertain significance |
| rs1488943045 | 17:37,262,175 | G/A | — | uncertain significance |
| rs938034150 | 17:37,263,697 | A/G | — | uncertain significance |
| rs772805966 | 17:37,263,728 | C/T | — | uncertain significance |
| rs2508879190 | 17:37,263,737 | C/G | — | uncertain significance |
| rs750109112 | 17:37,264,406 | C/T | — | uncertain significance |
| rs770095514 | 17:37,265,181 | G/A | — | uncertain significance |
| rs1389784584 | 17:37,265,204 | A/G | — | uncertain significance |
| rs1186887881 | 17:37,265,507 | C/G | — | uncertain significance |
| rs8064625 | 17:37,265,511 | C/T | — | uncertain significance |
| rs143773186 | 17:37,265,512 | G/A | — | uncertain significance |
| rs201093957 | 17:37,265,553 | C/T | — | likely benign |
| rs761194825 | 17:37,265,586 | C/T | — | uncertain significance |
| rs752951676 | 17:37,265,616 | C/T | — | uncertain significance |
| rs779947234 | 17:37,265,635 | G/C | — | uncertain significance |
| rs995029204 | 17:37,266,888 | G/A | — | — |
| rs192695415 | 17:37,282,732 | C/A | intron variant | — |
| rs757389606 | 17:37,295,960 | C/T | — | uncertain significance |
| rs376315498 | 17:37,295,962 | A/G | — | uncertain significance |
| rs114297422 | 17:37,296,025 | C/T | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.