ZC3H12B
zinc finger CCCH-type containing 12B
Summary
The protein encoded by this gene belongs to a family of CCCH-type zinc finger proteins that are involved in the proinflammatory activation of macrophages. The exact function of this family member is unknown, but it is thought to function as a ribonuclease. [provided by RefSeq, May 2010]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs144657889 | X:64,274,441 | G/A | intergenic variant | — |
| rs112433648 | X:64,329,955 | T/A | intergenic variant | — |
| rs148644956 | X:64,343,904 | A/T | — | — |
| rs7064929 | X:64,367,019 | G/A | intergenic variant | — |
| rs5964416 | X:64,368,487 | C/T | — | — |
| rs182625316 | X:64,390,074 | G/C | intergenic variant | — |
| rs140764915 | X:64,392,772 | T/G | intergenic variant | — |
| rs6624142 | X:64,405,169 | T/C | coding sequence variant | — |
| rs187953940 | X:64,458,848 | G/T | intergenic variant | — |
| rs762009949 | X:64,481,577 | C/G | — | — |
| rs149658894 | X:64,485,235 | C/T | intergenic variant | — |
| rs138463602 | X:64,496,703 | G/A | downstream gene variant | — |
| rs777649975 | X:64,504,369 | C/T | — | — |
| rs149434513 | X:64,510,099 | A/G | intergenic variant | — |
| rs5918938 | X:64,536,543 | T/A | — | — |
| rs188345773 | X:64,568,017 | G/A | intergenic variant | — |
| rs72627604 | X:64,568,985 | A/T | intergenic variant | — |
| rs72627605 | X:64,576,306 | T/A | — | — |
| rs145933839 | X:64,587,399 | A/G | intergenic variant | — |
| rs144195812 | X:64,601,070 | C/T | intergenic variant | — |
| rs182446246 | X:64,601,596 | A/T | intergenic variant | — |
| rs2213532 | X:64,605,332 | C/T | intergenic variant | — |
| rs5918944 | X:64,606,093 | A/G | intergenic variant | — |
| rs112681238 | X:64,612,099 | T/A | — | — |
| rs6653214 | X:64,614,820 | G/C | — | — |
| rs5964965 | X:64,617,013 | G/A | intergenic variant | — |
| rs5918947 | X:64,625,441 | C/G | — | — |
| rs4621963 | X:64,669,919 | A/G | intergenic variant | — |
| rs4592171 | X:64,669,938 | A/C | — | — |
| rs780707264 | X:64,708,739 | G/A | — | uncertain significance |
| rs749000283 | X:64,708,800 | T/C | — | uncertain significance |
| rs199856860 | X:64,708,833 | T/C | — | uncertain significance |
| rs773241007 | X:64,708,871 | G/T | — | uncertain significance |
| rs2522348346 | X:64,708,908 | C/T | — | uncertain significance |
| rs187793111 | X:64,708,944 | G/A | — | likely benign |
| rs192520287 | X:64,709,007 | A/G | — | benign |
| rs2522419973 | X:64,721,954 | C/T | — | uncertain significance |
| rs191189996 | X:64,721,970 | G/A | — | benign |
| rs747257073 | X:64,722,000 | C/G | — | uncertain significance |
| rs368700710 | X:64,722,008 | C/T | — | conflicting classifications of pathogenicity |
| rs2522422234 | X:64,722,184 | A/C | — | uncertain significance |
| rs776451042 | X:64,722,308 | G/A | — | uncertain significance |
| rs772644610 | X:64,722,334 | C/T | — | uncertain significance |
| rs369883605 | X:64,722,412 | G/A | — | uncertain significance |
| rs753303498 | X:64,722,448 | C/G | — | uncertain significance |
| rs756665932 | X:64,722,463 | C/T | — | likely benign |
| rs2522425199 | X:64,722,503 | A/G | — | uncertain significance |
| rs2522425277 | X:64,722,511 | G/A | — | uncertain significance |
| rs760832460 | X:64,722,697 | T/C | — | uncertain significance |
| rs765480548 | X:64,722,725 | G/A | — | uncertain significance |
| rs2522427648 | X:64,722,732 | A/G | — | likely benign |
| rs985114779 | X:64,722,794 | C/T | — | conflicting classifications of pathogenicity |
| rs190441107 | X:64,722,915 | G/A | — | uncertain significance |
| rs776883982 | X:64,722,999 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.