CLIC6
chloride intracellular channel 6
Summary
This gene encodes a member of the chloride intracellular channel family of proteins. The gene is part of a large triplicated region found on chromosomes 1, 6, and 21. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2015]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1046187866 | 21:36,041,725 | G/A | — | uncertain significance |
| rs1052078668 | 21:36,041,776 | A/T | — | uncertain significance |
| rs1301743676 | 21:36,041,815 | G/C | — | likely benign |
| rs186952765 | 21:36,041,820 | G/C | — | uncertain significance |
| rs1004284755 | 21:36,041,865 | G/T | — | uncertain significance |
| rs2516704610 | 21:36,041,914 | C/T | — | uncertain significance |
| rs1475952106 | 21:36,041,917 | G/C | — | uncertain significance |
| rs927788428 | 21:36,041,928 | G/A | — | uncertain significance |
| rs903063791 | 21:36,041,935 | C/T | — | uncertain significance |
| rs1032817233 | 21:36,041,970 | G/A | — | uncertain significance |
| rs1165128795 | 21:36,041,997 | G/A | — | likely benign |
| rs1298114288 | 21:36,042,024 | C/T | — | uncertain significance |
| rs1023371257 | 21:36,042,102 | G/A | — | uncertain significance |
| rs192051474 | 21:36,042,158 | G/A | — | likely benign |
| rs2516705303 | 21:36,042,163 | G/A | — | uncertain significance |
| rs1343412139 | 21:36,042,197 | A/G | — | uncertain significance |
| rs752208168 | 21:36,042,218 | C/G | — | likely benign |
| rs201318042 | 21:36,042,225 | G/T | — | benign |
| rs747194136 | 21:36,042,227 | A/G | — | likely benign |
| rs769814618 | 21:36,042,262 | C/A | — | uncertain significance |
| rs1989508054 | 21:36,042,296 | G/C | — | uncertain significance |
| rs1989509304 | 21:36,042,328 | G/T | — | uncertain significance |
| rs1320787221 | 21:36,042,338 | G/C | — | likely benign |
| rs770619828 | 21:36,042,346 | T/C | — | uncertain significance |
| rs1989510609 | 21:36,042,351 | G/A | — | uncertain significance |
| rs531747205 | 21:36,042,354 | G/A | — | uncertain significance |
| rs759120623 | 21:36,042,369 | G/A | — | uncertain significance |
| rs1451452977 | 21:36,042,380 | C/G | — | uncertain significance |
| rs1477395776 | 21:36,042,409 | A/G | — | uncertain significance |
| rs763696583 | 21:36,042,422 | G/C | — | likely benign |
| rs1165317342 | 21:36,042,440 | G/C | — | uncertain significance |
| rs62213790 | 21:36,042,470 | A/G | — | likely benign |
| rs1989520394 | 21:36,042,474 | G/A | — | uncertain significance |
| rs770904205 | 21:36,042,534 | G/A | — | uncertain significance |
| rs1274332911 | 21:36,042,619 | T/C | — | likely benign |
| rs975557601 | 21:36,042,638 | G/T | — | uncertain significance |
| rs148914738 | 21:36,042,666 | G/A | — | uncertain significance |
| rs1269521810 | 21:36,042,713 | C/T | — | likely benign |
| rs1365852771 | 21:36,042,735 | G/T | — | likely benign |
| rs1009884829 | 21:36,042,805 | G/T | — | uncertain significance |
| rs61753641 | 21:36,042,808 | G/T | — | benign |
| rs1395533909 | 21:36,042,818 | C/A | — | uncertain significance |
| rs753118378 | 21:36,042,878 | C/A | — | uncertain significance |
| rs1269476443 | 21:36,042,889 | A/G | — | uncertain significance |
| rs375245256 | 21:36,042,890 | G/A | — | likely benign |
| rs757325338 | 21:36,042,904 | C/T | — | uncertain significance |
| rs61731615 | 21:36,042,994 | G/C | — | benign |
| rs187670208 | 21:36,043,001 | C/A | — | benign |
| rs367827261 | 21:36,043,014 | G/A | — | uncertain significance |
| rs748827685 | 21:36,043,033 | A/G | — | uncertain significance |
| rs768498822 | 21:36,043,042 | A/T | — | uncertain significance |
| rs7275340 | 21:36,061,995 | G/C | — | — |
| rs116910126 | 21:36,065,170 | G/C | intron variant | — |
| rs2154447 | 21:36,069,051 | A/G | intron variant | — |
| rs2186288 | 21:36,069,867 | G/T | — | — |
| rs186013554 | 21:36,079,628 | C/T | — | likely benign |
| rs755661243 | 21:36,079,645 | T/A | — | uncertain significance |
| rs148002160 | 21:36,080,249 | G/A | — | uncertain significance |
| rs150507239 | 21:36,080,273 | G/A | — | uncertain significance |
| rs2516736147 | 21:36,080,283 | C/G | — | uncertain significance |
| rs374436284 | 21:36,080,316 | C/T | — | uncertain significance |
| rs2516737046 | 21:36,081,006 | A/T | — | uncertain significance |
| rs150066189 | 21:36,081,021 | A/G | — | uncertain significance |
| rs143782194 | 21:36,081,024 | C/T | — | uncertain significance |
| rs61733872 | 21:36,081,037 | C/T | — | benign |
| rs751986325 | 21:36,081,050 | G/A | — | uncertain significance |
| rs777770990 | 21:36,081,074 | A/G | — | uncertain significance |
| rs376511276 | 21:36,081,723 | G/A | — | uncertain significance |
| rs1395454483 | 21:36,081,780 | G/A | — | uncertain significance |
| rs61748623 | 21:36,081,785 | C/T | — | benign |
| rs141470374 | 21:36,081,793 | C/T | — | uncertain significance |
| rs1568973957 | 21:36,088,629 | A/G | — | uncertain significance |
| rs115008561 | 21:36,088,638 | G/A | — | benign |
| rs2516743497 | 21:36,088,668 | G/A | — | uncertain significance |
| rs78180107 | 21:36,088,670 | A/G | — | benign |
| rs772153839 | 21:36,088,692 | C/T | — | uncertain significance |
| rs2516743565 | 21:36,088,695 | A/G | — | uncertain significance |
| rs145328525 | 21:36,088,720 | G/A | — | benign |
| rs776464087 | 21:36,088,740 | T/C | — | uncertain significance |
| rs183771003 | 21:36,088,759 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.