FETUB
fetuin B
Summary
The protein encoded by this gene is a member of the fetuin family, part of the cystatin superfamily of cysteine protease inhibitors. Fetuins have been implicated in several diverse functions, including osteogenesis and bone resorption, regulation of the insulin and hepatocyte growth factor receptors, and response to systemic inflammation. This protein may be secreted by cells. [provided by RefSeq, Jul 2008]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs189419706 | 3:186,352,173 | A/C | regulatory region variant | — |
| rs111993713 | 3:186,357,416 | A/G | upstream gene variant | — |
| rs764614441 | 3:186,358,293 | G/A | — | uncertain significance |
| rs112267492 | 3:186,358,297 | C/G | — | benign |
| rs148037844 | 3:186,358,298 | G/A | — | uncertain significance |
| rs527318265 | 3:186,358,314 | C/A | — | uncertain significance |
| rs76555921 | 3:186,358,315 | C/A | — | benign |
| rs201789536 | 3:186,358,359 | A/T | — | uncertain significance |
| rs2473724315 | 3:186,358,382 | G/A | — | uncertain significance |
| rs146913398 | 3:186,358,454 | G/A | — | uncertain significance |
| rs370379105 | 3:186,358,458 | C/T | — | likely benign |
| rs765038127 | 3:186,358,820 | G/A | — | likely benign |
| rs779921072 | 3:186,358,888 | A/G | — | uncertain significance |
| rs373009962 | 3:186,358,907 | G/A | — | uncertain significance |
| rs143032930 | 3:186,358,937 | C/T | — | benign |
| rs1579036306 | 3:186,360,324 | C/T | — | uncertain significance |
| rs141401279 | 3:186,360,342 | G/A | — | uncertain significance |
| rs775043391 | 3:186,362,624 | C/T | — | uncertain significance |
| rs199634697 | 3:186,362,632 | G/A | — | uncertain significance |
| rs78581831 | 3:186,362,643 | G/A | — | likely benign |
| rs148507156 | 3:186,362,658 | G/A | — | benign |
| rs6785067 | 3:186,364,046 | G/A | missense variant | — |
| rs73886004 | 3:186,364,069 | C/T | — | benign |
| rs79014333 | 3:186,368,539 | C/T | intron variant | — |
| rs143617617 | 3:186,369,038 | G/A | — | benign |
| rs1718010599 | 3:186,369,055 | T/A | — | uncertain significance |
| rs1480334981 | 3:186,369,059 | T/C | — | uncertain significance |
| rs1389469906 | 3:186,370,058 | G/T | — | uncertain significance |
| rs142401278 | 3:186,370,142 | C/A | — | uncertain significance |
| rs139374439 | 3:186,370,207 | T/C | — | benign |
| rs374722004 | 3:186,370,266 | C/T | — | uncertain significance |
| rs748755333 | 3:186,370,362 | G/A | — | uncertain significance |
| rs1579059328 | 3:186,370,382 | C/G | — | uncertain significance |
| rs2473774628 | 3:186,370,383 | C/T | — | uncertain significance |
| rs116030393 | 3:186,370,407 | T/C | missense variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.