Gene entry
ARID1B
AT-rich interaction domain 1B
- Chromosome
- 6
- Cytoband
- 6q25.3
- Variants (rsID)
- 104
ARID1B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6q25.3). Its official name is “AT-rich interaction domain 1B”. The reference table lists 104 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs150140314Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Coffin-Siris syndrome 1
- rs3734441Benignsingle nucleotide variantHistory of neurodevelopmental disorder|Coffin-Siris syndrome 1
- rs387907141Pathogenicsingle nucleotide variantCoffin-Siris syndrome 1|ARID1B-related BAFopathy
- rs387907144Pathogenicsingle nucleotide variantCoffin-Siris syndrome 1|Inborn genetic diseases|ARID1B-related BAFopathy
- rs879253746PathogenicDuplication6 conditions|Coffin-Siris syndrome 1
- rs886041878PathogenicDuplicationCoffin-Siris syndrome 1
Other listed variants
- rs157661
- rs158258
- rs284416
- rs287928
- rs287945
- rs1535092
- rs2183462
- rs2236421
- rs4403273
- rs4869907
- rs4870491
- rs4870497
- rs6557536
- rs6906983
- rs6909426
- rs6912032
- rs6912237
- rs6927409
- rs6935886
- rs6941159
- rs6941976
- rs7751698
- rs7760326
- rs7770330
- rs9371447
- rs9371449
- rs9384502
- rs9384525
- rs9384527
- rs9397971
- rs9397973
- rs9478745
- rs9478751
- rs9480390
- rs9480424
- rs9480425
- rs9480436
- rs9480443
- rs9480447
- rs9885972
- rs11961360
- rs12196215
- rs12197388
- rs12526656
- rs12664986
- rs13215338
- rs17087983
- rs17087995
- rs17088067
- rs17088104
- rs17320572
- rs57586934
- rs73003497
- rs73020050
- rs73021541
- rs73581983
- rs74566821
- rs74814236
- rs75599866
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.