ZSCAN12
zinc finger and SCAN domain containing 12
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7754960 | 6:28,346,945 | G/T | — | — |
| rs67981811 | 6:28,354,835 | C/G | intron variant | — |
| rs36092177 | 6:28,357,807 | C/T | intron variant | — |
| rs13213986 | 6:28,358,009 | T/A | intron variant | — |
| rs183803005 | 6:28,358,260 | G/A | — | uncertain significance |
| rs753017905 | 6:28,358,334 | C/T | — | uncertain significance |
| rs745995535 | 6:28,358,364 | A/C | — | uncertain significance |
| rs760897310 | 6:28,358,422 | C/T | — | uncertain significance |
| rs772931627 | 6:28,358,519 | C/G | — | uncertain significance |
| rs376910254 | 6:28,358,553 | G/A | — | uncertain significance |
| rs2480826261 | 6:28,358,607 | T/C | — | uncertain significance |
| rs769781248 | 6:28,358,608 | G/A | — | uncertain significance |
| rs538120898 | 6:28,358,650 | C/T | — | uncertain significance |
| rs761237679 | 6:28,358,667 | T/A | — | uncertain significance |
| rs376896753 | 6:28,358,841 | G/A | — | uncertain significance |
| rs374427653 | 6:28,358,874 | C/T | — | uncertain significance |
| rs937092821 | 6:28,358,916 | T/C | — | uncertain significance |
| rs374273783 | 6:28,358,940 | T/C | — | uncertain significance |
| rs1760808698 | 6:28,358,971 | C/A | — | uncertain significance |
| rs1303735989 | 6:28,359,021 | T/C | — | uncertain significance |
| rs1233724848 | 6:28,359,081 | G/A | — | uncertain significance |
| rs558767625 | 6:28,359,106 | T/G | — | uncertain significance |
| rs866350017 | 6:28,359,132 | C/T | — | uncertain significance |
| rs766285213 | 6:28,359,138 | G/T | — | uncertain significance |
| rs751236815 | 6:28,359,154 | C/T | — | uncertain significance |
| rs370048592 | 6:28,359,327 | G/A | — | uncertain significance |
| rs184616997 | 6:28,359,382 | G/C | — | uncertain significance |
| rs374479373 | 6:28,359,430 | A/G | — | uncertain significance |
| rs1189882164 | 6:28,360,705 | G/A | — | uncertain significance |
| rs772375436 | 6:28,360,775 | G/C | — | uncertain significance |
| rs78680299 | 6:28,364,027 | A/G | — | — |
| rs750713503 | 6:28,365,783 | G/C | — | uncertain significance |
| rs1419321682 | 6:28,365,831 | C/T | — | uncertain significance |
| rs201689283 | 6:28,365,833 | A/G | — | likely benign |
| rs769700947 | 6:28,365,866 | A/C | — | uncertain significance |
| rs762954476 | 6:28,365,873 | C/G | — | uncertain significance |
| rs1437347061 | 6:28,366,002 | G/A | — | uncertain significance |
| rs777879883 | 6:28,366,080 | G/A | — | uncertain significance |
| rs891601328 | 6:28,366,179 | C/G | — | uncertain significance |
| rs35883476 | 6:28,368,508 | G/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.