ARID1B Chromosome 6

AT-rich interaction domain 1B
625 variants 625 Health Risk

Upload your DNA to see your personal genotypes for variants in ARID1B.

What This Gene Does
This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]
Gene Info
Gene Group
"AT-rich interaction domain containing|Armadillo like helical domain containing|BAF complex subunits"
Locus Type
gene with protein product
Location
6q25.3
Ensembl
ENSG00000049618
Associated Conditions (42)
Inborn genetic diseases
Coffin-Siris syndrome 1
Coffin-Siris syndrome
ARID1B-related disorder
See cases
ARID1B-related BAFopathy
Intellectual disability
Coffin Siris/Intellectual Disability
Microcephaly
Neurodevelopmental delay
Hereditary ataxia
6 conditions
Neoplasm
dysmorphy
intellectual deficiency
Marfanoid habitus and intellectual disability
Hirsutism
Wiedemann-Steiner syndrome
Neurodevelopmental disorder
Congenital cerebellar hypoplasia
+22 more conditions
Key Variants
All Variants (625)
RSID Category Clinical Significance Conditions
RS1554237992 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554238035 Health Risk Pathogenic Inborn genetic diseases, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1554238072 Health Risk Pathogenic Coffin-Siris syndrome 1, Inborn genetic diseases, Coffin-Siris syndrome 1
RS1554238093 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1554238124 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554238125 Health Risk Pathogenic
RS1554247637 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1554247662 Health Risk Pathogenic
RS1554248082 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554248137 Health Risk Pathogenic
RS1554248228 Health Risk Pathogenic
RS1554248236 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554248273 Health Risk Pathogenic
RS1554256703 Health Risk Pathogenic Inborn genetic diseases, Coffin-Siris syndrome 1, ARID1B-related BAFopathy
RS1554265253 Health Risk Pathogenic ARID1B-related BAFopathy, ARID1B-related BAFopathy
RS1554265269 Health Risk Pathogenic
RS1554265271 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1554265275 Health Risk Pathogenic Coffin-Siris syndrome 1, Intellectual disability, Coffin-Siris syndrome 1
RS1554265306 Health Risk Pathogenic
RS1554265316 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554265319 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554270831 Health Risk Pathogenic
RS1554294593 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554294665 Health Risk Pathogenic
RS1554294674 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554294698 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554298232 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554301230 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1554301257 Health Risk Pathogenic Autism spectrum disorder, Coffin-Siris syndrome 1, Autism spectrum disorder
RS1562328476 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1562328526 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1562331655 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1562345819 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1562347066 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1562352435 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1562355401 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1583026682 Health Risk Pathogenic
RS1583026884 Health Risk Pathogenic
RS1583279842 Health Risk Pathogenic
RS1583280152 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1583368813 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1583438967 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1583439013 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1583451360 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome, Coffin-Siris syndrome 1
RS1583464090 Health Risk Pathogenic
RS1583469151 Health Risk Pathogenic
RS1583479670 Health Risk Pathogenic
RS1583479817 Health Risk Pathogenic
RS1583480465 Health Risk Pathogenic
RS1583491381 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
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