WNT7A
Wnt family member 7A
Summary
This gene is a member of the WNT gene family, which consists of structurally related genes that encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is involved in the development of the anterior-posterior axis in the female reproductive tract, and also plays a critical role in uterine smooth muscle pattering and maintenance of adult uterine function. Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes. [provided by RefSeq, Jul 2008]
Known Variants88 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1124480 | 3:13,857,969 | T/C | 3 prime UTR variant | — |
| rs189888897 | 3:13,860,309 | G/A | — | likely benign |
| rs763687034 | 3:13,860,455 | A/G | — | uncertain significance |
| rs147606485 | 3:13,860,462 | C/T | — | likely benign |
| rs140491601 | 3:13,860,463 | G/A | — | conflicting classifications of pathogenicity |
| rs2470220430 | 3:13,860,510 | C/G | — | uncertain significance |
| rs774801091 | 3:13,860,549 | G/A | — | likely benign |
| rs561275177 | 3:13,860,554 | A/G | — | conflicting classifications of pathogenicity |
| rs761438329 | 3:13,860,572 | T/A | — | uncertain significance |
| rs748441283 | 3:13,860,600 | C/T | — | likely benign |
| rs957235068 | 3:13,860,607 | T/C | — | uncertain significance |
| rs104893835 | 3:13,860,617 | G/A | missense variant | pathogenic |
| rs149962459 | 3:13,860,630 | C/T | — | conflicting classifications of pathogenicity |
| rs1366112962 | 3:13,860,664 | T/A | — | uncertain significance |
| rs942840253 | 3:13,860,668 | G/A | — | uncertain significance |
| rs1694069385 | 3:13,860,670 | G/C | — | uncertain significance |
| rs2470220739 | 3:13,860,680 | T/C | — | uncertain significance |
| rs181440032 | 3:13,860,714 | C/T | — | benign |
| rs1047048047 | 3:13,860,744 | G/T | — | likely benign |
| rs1559293096 | 3:13,860,758 | G/A | — | uncertain significance |
| rs79543742 | 3:13,860,810 | C/T | — | benign |
| rs1559293147 | 3:13,860,826 | C/T | — | uncertain significance |
| rs397514643 | 3:13,860,827 | G/A | missense variant | pathogenic |
| rs143102670 | 3:13,860,867 | C/T | — | likely benign |
| rs387907231 | 3:13,860,881 | C/T | missense variant | pathogenic |
| rs1341360437 | 3:13,860,919 | A/G | — | uncertain significance |
| rs569287841 | 3:13,860,929 | G/C | — | likely benign |
| rs74932997 | 3:13,860,935 | G/A | — | benign |
| rs79020924 | 3:13,860,957 | A/G | — | benign |
| rs56300905 | 3:13,892,341 | G/A | regulatory region variant | — |
| rs3762721 | 3:13,895,806 | T/C | — | benign |
| rs3762720 | 3:13,895,817 | G/C | — | benign |
| rs116400918 | 3:13,895,950 | C/T | — | likely benign |
| rs768019460 | 3:13,896,043 | C/T | — | uncertain significance |
| rs149363953 | 3:13,896,044 | G/A | — | conflicting classifications of pathogenicity |
| rs201829729 | 3:13,896,068 | C/T | — | likely benign |
| rs772935313 | 3:13,896,112 | C/T | — | uncertain significance |
| rs767445224 | 3:13,896,125 | G/A | — | likely benign |
| rs199592697 | 3:13,896,129 | C/T | — | conflicting classifications of pathogenicity |
| rs917713880 | 3:13,896,130 | G/A | — | uncertain significance |
| rs3762719 | 3:13,896,140 | A/G | — | benign |
| rs748092973 | 3:13,896,167 | G/A | — | likely benign |
| rs759663787 | 3:13,896,191 | C/T | — | likely benign |
| rs367697256 | 3:13,896,200 | G/A | — | likely benign |
| rs2470260408 | 3:13,896,209 | G/T | — | uncertain significance |
| rs144536868 | 3:13,896,212 | G/A | — | benign |
| rs751287942 | 3:13,896,228 | G/A | — | uncertain significance |
| rs762400595 | 3:13,896,268 | T/C | — | uncertain significance |
| rs104893832 | 3:13,896,274 | C/T | missense variant | pathogenic |
| rs12639607 | 3:13,896,284 | C/T | — | benign |
| rs879255548 | 3:13,896,295 | G/A | missense variant | pathogenic |
| rs76778829 | 3:13,916,404 | G/A | — | likely benign |
| rs3749319 | 3:13,916,407 | G/T | — | benign |
| rs115457407 | 3:13,916,420 | G/A | — | likely benign |
| rs372068266 | 3:13,916,473 | C/T | — | uncertain significance |
| rs1433878302 | 3:13,916,483 | G/A | — | likely benign |
| rs756214872 | 3:13,916,510 | G/A | — | likely benign |
| rs397514666 | 3:13,916,528 | C/T | missense variant | pathogenic |
| rs75651130 | 3:13,916,529 | G/A | — | conflicting classifications of pathogenicity |
| rs766374751 | 3:13,916,571 | G/A | — | likely benign |
| rs757304251 | 3:13,916,593 | G/A | — | uncertain significance |
| rs200415711 | 3:13,916,596 | C/T | — | uncertain significance |
| rs1290597204 | 3:13,916,597 | G/A | — | uncertain significance |
| rs767232185 | 3:13,916,643 | G/A | — | likely benign |
| rs74784274 | 3:13,916,661 | G/A | — | likely benign |
| rs35103037 | 3:13,916,667 | G/A | — | likely benign |
| rs886044627 | 3:13,916,678 | G/A | — | uncertain significance |
| rs76480769 | 3:13,916,680 | G/A | — | benign |
| rs41284007 | 3:13,916,794 | G/T | — | benign |
| rs75079028 | 3:13,916,972 | C/T | — | likely benign |
| rs73151668 | 3:13,920,594 | G/T | regulatory region variant | — |
| rs73023640 | 3:13,921,032 | C/G | — | likely benign |
| rs113872063 | 3:13,921,143 | T/G | — | likely benign |
| rs76365041 | 3:13,921,254 | G/A | — | likely benign |
| rs769956705 | 3:13,921,260 | C/T | — | uncertain significance |
| rs145718587 | 3:13,921,289 | G/A | — | likely benign |
| rs1165912066 | 3:13,921,306 | C/T | — | uncertain significance |
| rs568644912 | 3:13,921,436 | C/A | — | likely benign |
| rs73151669 | 3:13,921,477 | G/T | — | benign |
| rs112325129 | 3:13,921,481 | A/G | — | likely benign |
| rs577047178 | 3:13,921,549 | C/T | — | likely benign |
| rs545716574 | 3:13,921,583 | G/C | — | likely benign |
| rs374634743 | 3:13,921,659 | G/T | — | benign |
| rs150614576 | 3:13,921,726 | C/G | — | likely benign |
| rs116220121 | 3:13,921,743 | G/T | — | likely benign |
| rs111360058 | 3:13,921,769 | C/T | — | likely benign |
| rs34268746 | 3:13,921,823 | C/T | — | benign |
| rs111437613 | 3:13,921,824 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.