ZSCAN9
zinc finger and SCAN domain containing 9
Summary
Enables sequence-specific double-stranded 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 Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs77793619 | 6:28,192,122 | C/A | — | — |
| rs1176539116 | 6:28,194,914 | G/T | — | uncertain significance |
| rs371694763 | 6:28,195,064 | G/A | — | uncertain significance |
| rs1453584496 | 6:28,195,185 | T/C | — | uncertain significance |
| rs2481129561 | 6:28,195,204 | A/C | — | uncertain significance |
| rs766689338 | 6:28,195,227 | A/G | — | uncertain significance |
| rs749870540 | 6:28,195,502 | G/A | — | uncertain significance |
| rs765050804 | 6:28,195,538 | T/G | — | uncertain significance |
| rs2481131680 | 6:28,195,550 | C/T | — | uncertain significance |
| rs34787248 | 6:28,197,886 | C/T | intron variant | — |
| rs2481140848 | 6:28,198,183 | C/G | — | uncertain significance |
| rs1760266050 | 6:28,198,219 | T/C | — | uncertain significance |
| rs150501877 | 6:28,200,409 | A/G | — | uncertain significance |
| rs2481149411 | 6:28,200,432 | A/G | — | uncertain significance |
| rs1760349208 | 6:28,200,471 | G/A | — | uncertain significance |
| rs546391720 | 6:28,200,574 | G/T | — | uncertain significance |
| rs1760355558 | 6:28,200,580 | T/C | — | uncertain significance |
| rs771195135 | 6:28,200,594 | A/G | — | uncertain significance |
| rs139661640 | 6:28,200,673 | G/A | — | likely benign |
| rs145267128 | 6:28,200,714 | T/C | — | uncertain significance |
| rs769054001 | 6:28,200,819 | C/T | — | uncertain significance |
| rs140538924 | 6:28,200,820 | G/A | — | uncertain significance |
| rs1038896214 | 6:28,200,862 | G/A | — | uncertain significance |
| rs780261805 | 6:28,200,886 | G/A | — | uncertain significance |
| rs138497434 | 6:28,200,895 | T/G | — | uncertain significance |
| rs775167071 | 6:28,200,918 | C/T | — | uncertain significance |
| rs13204012 | 6:28,201,531 | G/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.