ZNF512
zinc finger protein 512
Summary
This gene encodes a protein containing four putative zinc finger motifs. Zinc finger motifs may bind to proteins or nucleic acids. Zinc finger-containing proteins are involved in a variety of processes, including regulation of transcription. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs62138964 | 2:27,814,438 | C/T | intron variant | — |
| rs13022873 | 2:27,815,510 | A/T | — | — |
| rs13010586 | 2:27,817,817 | G/C | — | — |
| rs62138966 | 2:27,819,172 | G/A | intron variant | — |
| rs1266895701 | 2:27,820,980 | A/G | — | uncertain significance |
| rs774993134 | 2:27,821,113 | A/G | — | uncertain significance |
| rs12989678 | 2:27,821,482 | C/A | — | — |
| rs1302650916 | 2:27,822,473 | G/C | — | uncertain significance |
| rs2466365296 | 2:27,822,474 | G/A | — | uncertain significance |
| rs2466376383 | 2:27,824,240 | T/A | — | uncertain significance |
| rs12467476 | 2:27,825,715 | T/G | — | — |
| rs767449999 | 2:27,826,008 | G/C | — | uncertain significance |
| rs376857818 | 2:27,830,736 | C/G | — | uncertain significance |
| rs138329866 | 2:27,830,776 | G/A | — | uncertain significance |
| rs771458241 | 2:27,830,777 | T/G | — | uncertain significance |
| rs2384656 | 2:27,832,055 | A/G | intron variant | — |
| rs74175068 | 2:27,833,502 | T/C | intron variant | — |
| rs34016998 | 2:27,833,687 | C/T | intron variant | — |
| rs12987055 | 2:27,834,152 | T/C | intron variant | — |
| rs78170284 | 2:27,835,082 | G/A | intron variant | — |
| rs13020949 | 2:27,836,605 | C/T | intron variant | — |
| rs2466442235 | 2:27,838,116 | C/T | — | uncertain significance |
| rs1881395 | 2:27,838,549 | G/A | intron variant | — |
| rs774844710 | 2:27,840,353 | C/T | — | uncertain significance |
| rs2466452042 | 2:27,840,410 | A/G | — | uncertain significance |
| rs4666002 | 2:27,840,640 | G/C | intron variant | — |
| rs201647456 | 2:27,844,029 | G/A | — | uncertain significance |
| rs750676630 | 2:27,844,144 | G/A | — | uncertain significance |
| rs2466468493 | 2:27,844,173 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.