VWC2
von Willebrand factor C domain containing 2
Summary
This gene encodes a secreted bone morphogenic protein antagonist. The encoded protein is possibly involved in neural function and development and may have a role in cell adhesion.[provided by RefSeq, Oct 2009]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79259707 | 7:49,812,564 | C/A | upstream gene variant | — |
| rs1311595827 | 7:49,815,057 | T/G | — | uncertain significance |
| rs201551578 | 7:49,815,181 | C/A | — | uncertain significance |
| rs1270887284 | 7:49,815,194 | G/T | — | uncertain significance |
| rs1488280722 | 7:49,815,228 | C/A | — | uncertain significance |
| rs1242221544 | 7:49,815,236 | G/C | — | uncertain significance |
| rs1013667086 | 7:49,815,249 | G/C | — | uncertain significance |
| rs180779550 | 7:49,815,304 | C/A | — | uncertain significance |
| rs1055606572 | 7:49,815,341 | G/A | — | uncertain significance |
| rs895738697 | 7:49,815,350 | G/A | — | uncertain significance |
| rs755757639 | 7:49,815,381 | C/T | — | uncertain significance |
| rs543106702 | 7:49,815,414 | A/G | — | uncertain significance |
| rs780020277 | 7:49,815,441 | C/G | — | uncertain significance |
| rs1788046833 | 7:49,815,609 | C/A | — | uncertain significance |
| rs2534718752 | 7:49,815,626 | T/A | — | uncertain significance |
| rs2534718944 | 7:49,815,650 | T/G | — | uncertain significance |
| rs2534719141 | 7:49,815,687 | A/G | — | uncertain significance |
| rs866218265 | 7:49,815,696 | G/A | — | uncertain significance |
| rs1041639793 | 7:49,815,711 | C/T | — | uncertain significance |
| rs2534719284 | 7:49,815,722 | T/C | — | uncertain significance |
| rs577397 | 7:49,821,324 | G/C | — | — |
| rs552631340 | 7:49,825,587 | T/C | — | — |
| rs375100335 | 7:49,842,307 | G/A | — | uncertain significance |
| rs55633081 | 7:49,863,017 | A/T | intron variant | — |
| rs17551043 | 7:49,865,151 | G/T | intron variant | — |
| rs149079306 | 7:49,951,653 | G/A | — | uncertain significance |
| rs375417945 | 7:49,951,741 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.