ZNF180
zinc finger protein 180
Summary
Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs771446661 | 19:44,980,741 | T/C | — | uncertain significance |
| rs1396643584 | 19:44,980,786 | A/T | — | uncertain significance |
| rs986765209 | 19:44,980,823 | T/A | — | uncertain significance |
| rs150840613 | 19:44,980,848 | C/T | — | uncertain significance |
| rs919798243 | 19:44,980,932 | C/T | — | uncertain significance |
| rs1600063625 | 19:44,980,950 | C/T | — | uncertain significance |
| rs757930483 | 19:44,981,020 | G/A | — | uncertain significance |
| rs145650538 | 19:44,981,155 | G/T | — | uncertain significance |
| rs1008237974 | 19:44,981,202 | C/G | — | uncertain significance |
| rs2513521901 | 19:44,981,205 | C/T | — | uncertain significance |
| rs1403610903 | 19:44,981,221 | A/G | — | uncertain significance |
| rs761815023 | 19:44,981,223 | G/A | — | uncertain significance |
| rs367678775 | 19:44,981,253 | G/A | — | uncertain significance |
| rs145899142 | 19:44,981,340 | A/G | — | uncertain significance |
| rs2513524440 | 19:44,981,509 | C/A | — | uncertain significance |
| rs368668361 | 19:44,981,517 | G/A | — | uncertain significance |
| rs753677923 | 19:44,981,547 | C/G | — | uncertain significance |
| rs367716460 | 19:44,981,555 | A/G | — | likely benign |
| rs1969938250 | 19:44,981,572 | T/G | — | uncertain significance |
| rs780866666 | 19:44,981,608 | A/G | — | uncertain significance |
| rs1364802453 | 19:44,981,691 | T/C | — | uncertain significance |
| rs751962566 | 19:44,981,749 | T/G | — | uncertain significance |
| rs200561645 | 19:44,981,751 | T/C | — | uncertain significance |
| rs1969950776 | 19:44,981,785 | C/T | — | uncertain significance |
| rs143627648 | 19:44,981,837 | G/A | — | likely benign |
| rs183743567 | 19:44,981,867 | G/C | — | uncertain significance |
| rs780505738 | 19:44,982,013 | G/A | — | uncertain significance |
| rs774253862 | 19:44,982,046 | G/A | — | uncertain significance |
| rs1213052535 | 19:44,982,067 | T/C | — | uncertain significance |
| rs1346369940 | 19:44,982,100 | C/T | — | uncertain significance |
| rs1194159858 | 19:44,982,169 | C/T | — | uncertain significance |
| rs772762783 | 19:44,982,172 | C/T | — | uncertain significance |
| rs749521642 | 19:44,982,226 | A/G | — | uncertain significance |
| rs1445261307 | 19:44,982,264 | T/C | — | uncertain significance |
| rs940055390 | 19:44,982,310 | C/A | — | uncertain significance |
| rs199597294 | 19:44,983,604 | A/C | — | uncertain significance |
| rs745569589 | 19:44,983,607 | A/G | — | uncertain significance |
| rs375641920 | 19:44,983,616 | T/C | — | uncertain significance |
| rs149257524 | 19:44,987,725 | A/G | intron variant | — |
| rs777069215 | 19:44,988,610 | C/T | — | uncertain significance |
| rs1970169114 | 19:44,988,629 | T/G | — | uncertain significance |
| rs181736183 | 19:44,989,257 | A/G | intron variant | — |
| rs544300143 | 19:44,995,152 | C/A | — | — |
| rs547628678 | 19:45,000,652 | T/C | intron variant | — |
| rs2513590350 | 19:45,001,374 | C/T | — | uncertain significance |
| rs190761882 | 19:45,001,385 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.