PLXDC2
plexin domain containing 2
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7094178 | 10:20,105,223 | G/A | regulatory region variant | — |
| rs538990155 | 10:20,106,013 | C/A | — | uncertain significance |
| rs772703697 | 10:20,106,016 | G/A | — | uncertain significance |
| rs760347802 | 10:20,106,022 | C/G | — | uncertain significance |
| rs2491398882 | 10:20,106,078 | C/A | — | uncertain significance |
| rs756344797 | 10:20,106,085 | A/G | — | likely benign |
| rs449584 | 10:20,126,067 | T/G | — | — |
| rs150903364 | 10:20,160,778 | G/A | intron variant | — |
| rs1018635 | 10:20,226,672 | T/C | intron variant | — |
| rs1409338 | 10:20,227,267 | A/G | intron variant | — |
| rs137878669 | 10:20,290,770 | C/T | — | uncertain significance |
| rs115833666 | 10:20,290,812 | C/T | — | benign |
| rs138761663 | 10:20,290,835 | G/A | — | likely benign |
| rs1835806907 | 10:20,335,799 | A/T | — | uncertain significance |
| rs749590025 | 10:20,335,804 | A/G | — | uncertain significance |
| rs2491879601 | 10:20,335,855 | A/C | — | uncertain significance |
| rs540394643 | 10:20,335,859 | G/A | — | uncertain significance |
| rs750994706 | 10:20,335,878 | A/G | — | uncertain significance |
| rs768383816 | 10:20,432,254 | G/A | — | uncertain significance |
| rs4634985 | 10:20,434,780 | T/G | — | — |
| rs267602435 | 10:20,436,765 | C/G | — | uncertain significance |
| rs1834100128 | 10:20,436,796 | C/A | — | uncertain significance |
| rs148566256 | 10:20,465,943 | C/A | — | uncertain significance |
| rs760354875 | 10:20,465,972 | C/A | — | uncertain significance |
| rs754188191 | 10:20,466,281 | G/A | — | uncertain significance |
| rs11011859 | 10:20,487,702 | A/C | — | — |
| rs2131857808 | 10:20,500,602 | T/C | — | uncertain significance |
| rs536226658 | 10:20,506,404 | G/A | — | likely benign |
| rs201940365 | 10:20,506,425 | C/T | — | uncertain significance |
| rs752472328 | 10:20,506,460 | A/G | — | uncertain significance |
| rs374351012 | 10:20,506,491 | G/A | — | uncertain significance |
| rs9633643 | 10:20,513,547 | C/A | — | — |
| rs73605614 | 10:20,529,470 | A/C | intron variant | — |
| rs2253500 | 10:20,531,795 | A/T | — | — |
| rs778339194 | 10:20,534,294 | G/T | — | uncertain significance |
| rs766051112 | 10:20,534,345 | A/T | — | uncertain significance |
| rs764473799 | 10:20,534,364 | C/T | — | uncertain significance |
| rs780161026 | 10:20,534,390 | A/C | — | uncertain significance |
| rs148113935 | 10:20,534,391 | T/C | — | uncertain significance |
| rs36003977 | 10:20,534,406 | C/T | — | uncertain significance |
| rs1571942 | 10:20,542,634 | A/G | intron variant | — |
| rs143829207 | 10:20,568,645 | G/A | — | uncertain significance |
| rs11011932 | 10:20,576,790 | C/T | 3 prime UTR variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.