VWA5B2
von Willebrand factor A domain containing 5B2
Known Variants79 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs180715817 | 3:183,948,153 | A/G | regulatory region variant | — |
| rs929455841 | 3:183,948,378 | G/C | — | uncertain significance |
| rs750637181 | 3:183,948,383 | T/C | — | uncertain significance |
| rs1387193581 | 3:183,948,392 | G/A | — | uncertain significance |
| rs1468229019 | 3:183,948,417 | G/A | — | uncertain significance |
| rs2473796802 | 3:183,948,542 | C/G | — | uncertain significance |
| rs1717323674 | 3:183,948,676 | G/A | — | uncertain significance |
| rs2473797567 | 3:183,948,681 | C/A | — | uncertain significance |
| rs1019447824 | 3:183,948,700 | C/T | — | uncertain significance |
| rs560850383 | 3:183,951,129 | G/T | — | likely benign |
| rs2473804823 | 3:183,951,176 | G/T | — | uncertain significance |
| rs532605712 | 3:183,951,181 | G/A | — | uncertain significance |
| rs776643359 | 3:183,951,408 | T/G | — | uncertain significance |
| rs571169902 | 3:183,951,465 | C/T | — | uncertain significance |
| rs866076856 | 3:183,951,488 | G/A | — | uncertain significance |
| rs2473808248 | 3:183,952,090 | C/G | — | uncertain significance |
| rs745953037 | 3:183,952,093 | C/T | — | uncertain significance |
| rs2473808327 | 3:183,952,098 | C/A | — | uncertain significance |
| rs757263553 | 3:183,952,131 | C/G | — | uncertain significance |
| rs1036792197 | 3:183,952,156 | G/A | — | uncertain significance |
| rs1717765685 | 3:183,952,420 | G/C | — | uncertain significance |
| rs749867062 | 3:183,952,481 | C/T | — | uncertain significance |
| rs781028398 | 3:183,952,538 | C/T | — | uncertain significance |
| rs896916338 | 3:183,952,996 | C/T | — | likely benign |
| rs1209912339 | 3:183,953,989 | A/G | — | uncertain significance |
| rs1442113047 | 3:183,954,007 | C/T | — | uncertain significance |
| rs1717979163 | 3:183,954,031 | A/C | — | uncertain significance |
| rs778106714 | 3:183,954,139 | G/T | — | likely benign |
| rs1337694929 | 3:183,954,159 | T/C | — | uncertain significance |
| rs1278516836 | 3:183,954,165 | C/T | — | uncertain significance |
| rs188099951 | 3:183,954,168 | T/C | — | uncertain significance |
| rs1298249935 | 3:183,954,218 | G/A | — | likely benign |
| rs1577090903 | 3:183,954,535 | A/G | — | uncertain significance |
| rs760764183 | 3:183,955,030 | G/A | — | uncertain significance |
| rs375332654 | 3:183,955,056 | G/A | — | uncertain significance |
| rs566967537 | 3:183,955,188 | C/T | — | uncertain significance |
| rs374687989 | 3:183,956,100 | C/A | — | uncertain significance |
| rs1445004876 | 3:183,956,122 | G/T | — | uncertain significance |
| rs551808149 | 3:183,956,127 | G/A | — | uncertain significance |
| rs932437783 | 3:183,956,160 | G/T | — | uncertain significance |
| rs368917489 | 3:183,956,411 | T/C | — | uncertain significance |
| rs767287777 | 3:183,956,417 | G/A | — | uncertain significance |
| rs1329689304 | 3:183,956,524 | T/A | — | uncertain significance |
| rs573085436 | 3:183,956,545 | G/A | — | uncertain significance |
| rs2473825858 | 3:183,956,555 | C/T | — | uncertain significance |
| rs1205060319 | 3:183,956,587 | C/T | — | uncertain significance |
| rs1718268642 | 3:183,956,609 | C/T | — | uncertain significance |
| rs577657610 | 3:183,957,260 | G/A | — | uncertain significance |
| rs73051619 | 3:183,957,315 | T/C | — | likely benign |
| rs759486696 | 3:183,957,323 | C/A | — | uncertain significance |
| rs2473829137 | 3:183,957,356 | G/A | — | uncertain significance |
| rs2473829767 | 3:183,957,536 | T/C | — | uncertain significance |
| rs763700356 | 3:183,957,591 | C/A | — | uncertain significance |
| rs1001777404 | 3:183,957,657 | T/G | — | uncertain significance |
| rs79321968 | 3:183,957,731 | G/T | — | uncertain significance |
| rs975796715 | 3:183,957,765 | T/C | — | uncertain significance |
| rs1718406550 | 3:183,957,785 | C/G | — | uncertain significance |
| rs542606490 | 3:183,957,810 | C/T | — | uncertain significance |
| rs1051721528 | 3:183,958,639 | C/T | — | uncertain significance |
| rs2473835125 | 3:183,958,665 | G/C | — | uncertain significance |
| rs2473835355 | 3:183,958,708 | G/T | — | uncertain significance |
| rs61750832 | 3:183,958,830 | G/A | — | uncertain significance |
| rs1560158335 | 3:183,959,007 | G/A | — | uncertain significance |
| rs1230019497 | 3:183,959,044 | G/A | — | uncertain significance |
| rs1350753948 | 3:183,959,053 | C/T | — | uncertain significance |
| rs1448641150 | 3:183,959,071 | C/A | — | uncertain significance |
| rs759256176 | 3:183,959,108 | C/G | — | uncertain significance |
| rs761864069 | 3:183,959,171 | C/A | — | uncertain significance |
| rs1239045501 | 3:183,959,492 | C/T | — | uncertain significance |
| rs1277221669 | 3:183,959,510 | G/A | — | uncertain significance |
| rs1718711335 | 3:183,959,561 | A/G | — | uncertain significance |
| rs1577098471 | 3:183,959,563 | G/A | — | uncertain significance |
| rs1391143333 | 3:183,959,584 | C/T | — | uncertain significance |
| rs779061272 | 3:183,959,587 | G/A | — | uncertain significance |
| rs759034432 | 3:183,959,629 | C/G | — | uncertain significance |
| rs911077626 | 3:183,959,650 | G/A | — | uncertain significance |
| rs532286690 | 3:183,959,669 | C/T | — | uncertain significance |
| rs1344104225 | 3:183,959,708 | C/T | — | uncertain significance |
| rs746947709 | 3:183,959,816 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.