IQCH
IQ motif containing H
Summary
Predicted to act upstream of or within lncRNA transcription and single fertilization. Predicted to be active in nuclear speck. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants70 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs58074225 | 15:67,545,892 | G/A | upstream gene variant | — |
| rs140241627 | 15:67,547,255 | C/T | — | benign |
| rs2140412927 | 15:67,547,258 | C/G | — | uncertain significance |
| rs377745050 | 15:67,547,262 | C/T | — | uncertain significance |
| rs8038652 | 15:67,552,064 | G/A | upstream gene variant | — |
| rs764427071 | 15:67,553,670 | G/A | — | likely benign |
| rs1232642249 | 15:67,553,683 | A/G | — | uncertain significance |
| rs754645263 | 15:67,555,464 | A/G | — | uncertain significance |
| rs149070596 | 15:67,555,466 | A/G | — | uncertain significance |
| rs12443279 | 15:67,561,355 | C/G | intron variant | — |
| rs12901789 | 15:67,562,214 | A/C | intron variant | — |
| rs1966257020 | 15:67,571,737 | C/T | — | uncertain significance |
| rs747452749 | 15:67,571,830 | C/T | — | uncertain significance |
| rs12440869 | 15:67,610,951 | A/G | — | — |
| rs373527321 | 15:67,629,313 | A/G | — | likely benign |
| rs2505373946 | 15:67,629,406 | C/T | — | uncertain significance |
| rs749121911 | 15:67,636,446 | G/A | — | likely benign |
| rs767445068 | 15:67,636,511 | C/T | — | uncertain significance |
| rs749070080 | 15:67,636,523 | A/G | — | likely benign |
| rs35688953 | 15:67,640,129 | T/C | intron variant | — |
| rs1342784527 | 15:67,652,186 | G/A | — | uncertain significance |
| rs2505507573 | 15:67,652,195 | G/A | — | likely benign |
| rs12915659 | 15:67,655,973 | G/T | — | — |
| rs8043060 | 15:67,661,784 | G/A | intron variant | — |
| rs35819343 | 15:67,661,850 | A/G | — | — |
| rs72745473 | 15:67,663,250 | A/T | — | — |
| rs775124649 | 15:67,664,462 | A/G | — | uncertain significance |
| rs1282228945 | 15:67,664,468 | C/T | — | uncertain significance |
| rs144013728 | 15:67,664,515 | G/T | — | uncertain significance |
| rs1316290190 | 15:67,664,574 | A/T | — | uncertain significance |
| rs34738407 | 15:67,664,610 | C/T | — | benign |
| rs753212872 | 15:67,664,705 | T/C | — | uncertain significance |
| rs34599707 | 15:67,664,713 | T/G | — | uncertain significance |
| rs1970577995 | 15:67,664,835 | G/C | — | uncertain significance |
| rs145795608 | 15:67,664,879 | A/G | — | uncertain significance |
| rs1970587668 | 15:67,664,978 | A/G | — | uncertain significance |
| rs1971065889 | 15:67,677,354 | T/G | — | uncertain significance |
| rs754328443 | 15:67,681,208 | T/C | — | likely benign |
| rs781207918 | 15:67,681,216 | G/A | — | uncertain significance |
| rs774781508 | 15:67,687,660 | T/G | — | uncertain significance |
| rs370046858 | 15:67,687,690 | A/T | — | uncertain significance |
| rs747787960 | 15:67,687,722 | G/A | — | uncertain significance |
| rs1468992867 | 15:67,687,758 | G/A | — | uncertain significance |
| rs1971434041 | 15:67,687,813 | A/G | — | uncertain significance |
| rs139553529 | 15:67,687,820 | C/T | — | likely benign |
| rs76782783 | 15:67,692,446 | T/G | — | benign |
| rs769242387 | 15:67,692,501 | G/A | — | uncertain significance |
| rs1047720643 | 15:67,692,543 | C/T | — | uncertain significance |
| rs35933176 | 15:67,692,566 | T/C | — | likely benign |
| rs7359257 | 15:67,702,907 | A/C | intron variant | — |
| rs751089797 | 15:67,709,354 | C/T | — | uncertain significance |
| rs28399271 | 15:67,710,011 | G/T | — | — |
| rs151170401 | 15:67,713,634 | G/A | — | uncertain significance |
| rs367833219 | 15:67,713,670 | A/C | — | uncertain significance |
| rs200639045 | 15:67,713,701 | A/G | — | uncertain significance |
| rs147731503 | 15:67,713,703 | G/A | — | uncertain significance |
| rs142614145 | 15:67,713,715 | G/A | — | uncertain significance |
| rs756324163 | 15:67,713,750 | C/A | — | uncertain significance |
| rs1201775604 | 15:67,713,803 | T/G | — | uncertain significance |
| rs746651653 | 15:67,713,836 | C/G | — | uncertain significance |
| rs2505805496 | 15:67,713,866 | T/G | — | uncertain significance |
| rs2081742904 | 15:67,713,877 | C/G | — | uncertain significance |
| rs370446454 | 15:67,757,579 | C/T | — | uncertain significance |
| rs2505982677 | 15:67,757,619 | G/A | — | likely benign |
| rs146237345 | 15:67,768,036 | G/A | — | uncertain significance |
| rs140009311 | 15:67,768,050 | G/A | — | uncertain significance |
| rs1040801439 | 15:67,768,077 | G/A | — | likely benign |
| rs142631355 | 15:67,768,084 | C/G | — | uncertain significance |
| rs367994255 | 15:67,782,376 | C/A | — | uncertain significance |
| rs1456243835 | 15:67,793,065 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.