CHD9
chromodomain helicase DNA binding protein 9
Summary
Predicted to enable several functions, including ATP binding activity; ATP hydrolysis activity; and DNA helicase activity. Predicted to be involved in chromatin organization. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants144 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs9931598 | 16:53,105,063 | T/G | — | — |
| rs577250106 | 16:53,152,130 | A/G | — | — |
| rs56088754 | 16:53,158,219 | A/G | intron variant | — |
| rs62047987 | 16:53,163,796 | T/C | intron variant | — |
| rs112757932 | 16:53,165,035 | A/C | — | — |
| rs12597502 | 16:53,170,069 | A/G | intron variant | — |
| rs62047990 | 16:53,171,664 | C/T | intron variant | — |
| rs8057569 | 16:53,173,233 | A/G | intron variant | — |
| rs8053357 | 16:53,179,492 | C/T | — | — |
| rs11859517 | 16:53,181,247 | C/T | intron variant | — |
| rs67499551 | 16:53,183,605 | T/A | intron variant | — |
| rs776868081 | 16:53,190,014 | A/T | — | uncertain significance |
| rs760520068 | 16:53,190,027 | T/C | — | uncertain significance |
| rs957041250 | 16:53,190,096 | C/T | — | uncertain significance |
| rs747697032 | 16:53,190,260 | G/A | — | uncertain significance |
| rs772666237 | 16:53,190,332 | C/T | — | uncertain significance |
| rs1030817891 | 16:53,190,336 | A/G | — | uncertain significance |
| rs1407297584 | 16:53,190,365 | A/C | — | uncertain significance |
| rs2545478407 | 16:53,190,443 | C/T | — | uncertain significance |
| rs754400242 | 16:53,190,501 | C/T | — | uncertain significance |
| rs2041538602 | 16:53,190,512 | C/A | — | uncertain significance |
| rs548090628 | 16:53,190,537 | C/T | — | uncertain significance |
| rs2545480751 | 16:53,190,659 | T/C | — | uncertain significance |
| rs772196014 | 16:53,190,702 | C/T | — | uncertain significance |
| rs377416139 | 16:53,190,707 | A/G | — | uncertain significance |
| rs374801460 | 16:53,190,872 | G/T | — | uncertain significance |
| rs758182260 | 16:53,190,896 | A/G | — | uncertain significance |
| rs762238500 | 16:53,190,981 | A/G | — | uncertain significance |
| rs748675330 | 16:53,191,050 | G/A | — | uncertain significance |
| rs763829620 | 16:53,191,101 | C/T | — | uncertain significance |
| rs1354843859 | 16:53,191,113 | T/C | — | uncertain significance |
| rs910296828 | 16:53,191,125 | A/G | — | uncertain significance |
| rs922732152 | 16:53,191,205 | A/C | — | uncertain significance |
| rs199866020 | 16:53,191,245 | T/G | — | uncertain significance |
| rs747733475 | 16:53,191,327 | G/A | — | likely benign |
| rs899704113 | 16:53,191,352 | A/G | — | uncertain significance |
| rs764468064 | 16:53,191,380 | C/T | — | uncertain significance |
| rs2041602098 | 16:53,191,439 | T/C | — | uncertain significance |
| rs7204230 | 16:53,192,331 | T/G | — | — |
| rs7189599 | 16:53,203,971 | G/C | — | — |
| rs7196485 | 16:53,203,977 | T/G | downstream gene variant | — |
| rs1279121582 | 16:53,243,395 | C/T | — | uncertain significance |
| rs2546129230 | 16:53,243,408 | G/T | — | uncertain significance |
| rs2546130276 | 16:53,243,442 | C/A | — | uncertain significance |
| rs373299221 | 16:53,243,523 | C/T | — | uncertain significance |
| rs1470712359 | 16:53,243,559 | C/T | — | uncertain significance |
| rs376323053 | 16:53,243,568 | C/T | — | uncertain significance |
| rs200843001 | 16:53,243,663 | A/G | — | likely benign |
| rs778589471 | 16:53,243,707 | A/G | — | uncertain significance |
| rs758566180 | 16:53,256,579 | A/G | — | uncertain significance |
| rs561020870 | 16:53,256,663 | C/T | — | uncertain significance |
| rs369540834 | 16:53,260,324 | A/G | — | uncertain significance |
| rs769534090 | 16:53,260,422 | G/C | — | uncertain significance |
| rs758676695 | 16:53,261,497 | T/A | — | uncertain significance |
| rs1002543995 | 16:53,265,559 | C/A | — | uncertain significance |
| rs2048194611 | 16:53,265,688 | A/G | — | uncertain significance |
| rs369035655 | 16:53,269,100 | C/T | — | uncertain significance |
| rs377741006 | 16:53,269,101 | G/A | — | uncertain significance |
| rs779862877 | 16:53,269,158 | A/G | — | uncertain significance |
| rs2546543270 | 16:53,272,371 | T/C | — | uncertain significance |
| rs2048815902 | 16:53,272,382 | G/A | — | uncertain significance |
| rs757538821 | 16:53,272,407 | C/T | — | uncertain significance |
| rs368563114 | 16:53,272,461 | T/C | — | uncertain significance |
| rs201710491 | 16:53,276,756 | G/A | — | uncertain significance |
| rs1437676492 | 16:53,276,812 | C/T | — | uncertain significance |
| rs374505230 | 16:53,276,849 | G/A | — | uncertain significance |
| rs2543442171 | 16:53,276,852 | G/C | — | uncertain significance |
| rs938008081 | 16:53,279,336 | T/G | — | uncertain significance |
| rs1216911371 | 16:53,279,675 | A/G | — | uncertain significance |
| rs746903228 | 16:53,279,714 | A/G | — | uncertain significance |
| rs373076192 | 16:53,281,375 | C/T | — | uncertain significance |
| rs192610097 | 16:53,283,788 | T/C | — | uncertain significance |
| rs2543636780 | 16:53,283,947 | A/G | — | uncertain significance |
| rs2543745585 | 16:53,288,353 | C/G | — | uncertain significance |
| rs2543746675 | 16:53,288,413 | C/T | — | uncertain significance |
| rs2543747569 | 16:53,288,440 | G/A | — | uncertain significance |
| rs2543781893 | 16:53,289,569 | G/A | — | uncertain significance |
| rs1318345762 | 16:53,289,572 | A/G | — | uncertain significance |
| rs2543782194 | 16:53,289,576 | T/C | — | uncertain significance |
| rs375916437 | 16:53,289,636 | G/A | — | uncertain significance |
| rs2050532534 | 16:53,289,649 | T/A | — | likely benign |
| rs372547335 | 16:53,296,990 | T/C | — | uncertain significance |
| rs759835455 | 16:53,301,266 | A/G | — | uncertain significance |
| rs750009284 | 16:53,301,327 | G/A | — | uncertain significance |
| rs1171102170 | 16:53,301,341 | C/T | — | uncertain significance |
| rs754761253 | 16:53,301,348 | A/G | — | uncertain significance |
| rs2544062942 | 16:53,302,016 | A/T | — | likely benign |
| rs369431664 | 16:53,302,018 | G/T | — | uncertain significance |
| rs778369780 | 16:53,307,631 | A/G | — | uncertain significance |
| rs73600045 | 16:53,315,180 | A/G | — | — |
| rs764360924 | 16:53,319,531 | A/G | — | uncertain significance |
| rs374132613 | 16:53,319,539 | C/T | — | uncertain significance |
| rs190545426 | 16:53,321,889 | A/T | — | uncertain significance |
| rs61754093 | 16:53,321,892 | A/G | — | likely benign |
| rs756375296 | 16:53,326,822 | A/G | — | uncertain significance |
| rs1381047417 | 16:53,326,847 | A/G | — | uncertain significance |
| rs1021173579 | 16:53,330,999 | A/G | — | uncertain significance |
| rs773225940 | 16:53,331,040 | C/T | — | uncertain significance |
| rs199568786 | 16:53,337,728 | A/G | — | uncertain significance |
| rs1206220443 | 16:53,337,730 | G/A | — | uncertain significance |
Showing 100 of 144 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.