WNT7B
Wnt family member 7B
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. Among members of the human WNT family, this gene product is most similar to WNT7A protein. [provided by RefSeq, Oct 2008]
Known Variants36 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775439780 | 22:46,318,756 | C/T | — | uncertain significance |
| rs201546829 | 22:46,318,879 | C/T | — | uncertain significance |
| rs151338959 | 22:46,318,883 | C/T | — | benign |
| rs61735041 | 22:46,318,884 | G/A | — | uncertain significance |
| rs2518215712 | 22:46,318,917 | T/C | — | uncertain significance |
| rs780469731 | 22:46,318,927 | C/T | — | uncertain significance |
| rs768571825 | 22:46,318,941 | G/A | — | uncertain significance |
| rs748420070 | 22:46,319,013 | C/T | — | uncertain significance |
| rs60537690 | 22:46,319,036 | G/T | — | benign |
| rs1475762618 | 22:46,319,047 | G/A | — | likely pathogenic |
| rs143921169 | 22:46,319,202 | C/T | — | uncertain significance |
| rs1158594747 | 22:46,326,986 | C/T | — | pathogenic |
| rs200797257 | 22:46,327,010 | T/G | — | uncertain significance |
| rs924061115 | 22:46,327,057 | C/T | — | uncertain significance |
| rs202130862 | 22:46,327,117 | G/T | — | uncertain significance |
| rs768926470 | 22:46,327,154 | C/T | — | uncertain significance |
| rs146315543 | 22:46,327,188 | G/A | — | likely benign |
| rs1297124801 | 22:46,327,210 | G/A | — | uncertain significance |
| rs145039496 | 22:46,336,571 | C/T | intron variant | — |
| rs1569119395 | 22:46,345,806 | G/A | — | pathogenic |
| rs147267470 | 22:46,345,837 | G/A | — | likely benign |
| rs1051933787 | 22:46,345,870 | C/G | — | uncertain significance |
| rs2146732713 | 22:46,345,873 | G/C | — | pathogenic |
| rs764176810 | 22:46,345,935 | G/A | — | uncertain significance |
| rs745544316 | 22:46,346,011 | C/A | — | likely benign |
| rs10453441 | 22:46,363,739 | A/C | — | — |
| rs9330813 | 22:46,364,161 | G/C | — | — |
| rs9330814 | 22:46,364,191 | C/A | — | — |
| rs570639864 | 22:46,365,137 | G/A | — | — |
| rs28971325 | 22:46,367,144 | G/A | regulatory region variant | — |
| rs62226057 | 22:46,368,130 | T/C | regulatory region variant | — |
| rs200329677 | 22:46,369,778 | C/T | — | — |
| rs73175081 | 22:46,371,079 | A/T | — | — |
| rs1932558961 | 22:46,372,590 | G/C | — | uncertain significance |
| rs774389678 | 22:46,372,599 | C/T | — | likely benign |
| rs75792643 | 22:46,372,968 | C/T | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.