Gene entry
CHD9
chromodomain helicase DNA binding protein 9
- Chromosome
- 16
- Cytoband
- 16q12.2
- Variants (rsID)
- 39
CHD9 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16q12.2). Its official name is “chromodomain helicase DNA binding protein 9”. The reference table lists 39 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
Other listed variants
- rs1073454
- rs1108574
- rs1420306
- rs3852742
- rs7204230
- rs8049859
- rs11860145
- rs12599832
- rs12708901
- rs12934164
- rs56285139
- rs59171343
- rs61747411
- rs62049787
- rs62050296
- rs72799625
- rs72799639
- rs73590888
- rs73599651
- rs73601686
- rs75866289
- rs75925643
- rs77255227
- rs77931115
- rs79231128
- rs80307327
- rs113104734
- rs113301402
- rs117149766
- rs117216872
- rs117599701
- rs118144862
- rs140795496
- rs141023143
- rs145196273
- rs145647209
- rs150289108
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
