CDYL2
chromodomain Y like 2
Summary
Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761338715 | 16:80,638,415 | C/T | — | uncertain significance |
| rs2507385423 | 16:80,638,434 | C/T | — | uncertain significance |
| rs1273478313 | 16:80,642,108 | G/A | — | uncertain significance |
| rs4613079 | 16:80,643,957 | G/C | — | — |
| rs368472250 | 16:80,646,531 | C/A | — | uncertain significance |
| rs115679401 | 16:80,646,676 | C/A | — | benign |
| rs1247897349 | 16:80,646,690 | C/G | — | uncertain significance |
| rs7500067 | 16:80,648,296 | A/G | regulatory region variant | — |
| rs13329835 | 16:80,650,805 | A/G | intron variant | — |
| rs370310225 | 16:80,654,679 | G/A | — | uncertain significance |
| rs1907047240 | 16:80,654,715 | C/T | — | uncertain significance |
| rs1907048831 | 16:80,654,736 | G/C | — | uncertain significance |
| rs368202024 | 16:80,654,810 | G/A | — | uncertain significance |
| rs757864703 | 16:80,654,817 | G/A | — | uncertain significance |
| rs761277499 | 16:80,666,944 | G/A | — | uncertain significance |
| rs1199289855 | 16:80,666,946 | C/A | — | uncertain significance |
| rs148307202 | 16:80,666,967 | C/T | — | benign |
| rs1286235006 | 16:80,667,049 | T/C | — | uncertain significance |
| rs373147588 | 16:80,667,070 | T/C | — | uncertain significance |
| rs2507431072 | 16:80,667,091 | A/G | — | uncertain significance |
| rs879863061 | 16:80,667,130 | G/T | — | uncertain significance |
| rs74794145 | 16:80,675,040 | T/C | intron variant | — |
| rs776512863 | 16:80,704,259 | G/A | — | — |
| rs368116348 | 16:80,718,453 | G/C | — | uncertain significance |
| rs373304541 | 16:80,718,502 | A/T | — | uncertain significance |
| rs373621157 | 16:80,718,563 | G/A | — | uncertain significance |
| rs562488396 | 16:80,718,652 | C/G | — | uncertain significance |
| rs1023081357 | 16:80,718,692 | T/C | — | uncertain significance |
| rs2507534074 | 16:80,718,698 | T/C | — | uncertain significance |
| rs750885476 | 16:80,718,710 | G/C | — | uncertain significance |
| rs746932115 | 16:80,718,764 | G/A | — | uncertain significance |
| rs376407812 | 16:80,718,800 | G/A | — | uncertain significance |
| rs761986882 | 16:80,718,834 | T/C | — | likely benign |
| rs1260993441 | 16:80,718,929 | G/A | — | uncertain significance |
| rs41472047 | 16:80,745,775 | G/A | intron variant | — |
| rs13329850 | 16:80,784,797 | C/G | intron variant | — |
| rs190103938 | 16:80,828,596 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.