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
RS1583491515 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1583500173 Health Risk Pathogenic
RS1583502875 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1583513716 Health Risk Pathogenic
RS1583515557 Health Risk Pathogenic
RS1583516200 Health Risk Pathogenic
RS1583518354 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1778877596 Health Risk Pathogenic
RS1778885211 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1778945620 Health Risk Pathogenic Inborn genetic diseases, ARID1B-related disorder, Inborn genetic diseases
RS1779009539 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1779015991 Health Risk Pathogenic Intellectual disability, Intellectual disability
RS1782980450 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1784850566 Health Risk Pathogenic
RS1786823829 Health Risk Pathogenic Intellectual disability, Intellectual disability
RS1786833331 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1788661091 Health Risk Pathogenic
RS1788925132 Health Risk Pathogenic
RS1788927433 Health Risk Pathogenic
RS1788932771 Health Risk Pathogenic
RS1789979659 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1789997179 Health Risk Pathogenic
RS1791374798 Health Risk Pathogenic Coffin-Siris syndrome 1, ARID1B-related BAFopathy, Coffin-Siris syndrome 1
RS1791379124 Health Risk Pathogenic
RS1791918216 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1791922830 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1792127580 Health Risk Pathogenic
RS1793228690 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1793246524 Health Risk Pathogenic
RS1793251352 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1793713030 Health Risk Pathogenic
RS1794053879 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1794071513 Health Risk Pathogenic
RS1794099468 Health Risk Pathogenic
RS1794276185 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1794278792 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1794468027 Health Risk Pathogenic
RS1794509686 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1794557198 Health Risk Pathogenic
RS1794563443 Health Risk Pathogenic Intellectual disability, Intellectual disability
RS1794569741 Health Risk Pathogenic Rare genetic intellectual disability, Rare genetic intellectual disability
RS1794570475 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS1794584714 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS201653711 Health Risk Pathogenic Inborn genetic diseases, Coffin-Siris syndrome 1, Inborn genetic diseases
RS2114999746 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS2115000174 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
RS2115003519 Health Risk Pathogenic See cases, See cases
RS2115003731 Health Risk Pathogenic
RS2128046981 Health Risk Pathogenic
RS2128210848 Health Risk Pathogenic Coffin-Siris syndrome 1, Coffin-Siris syndrome 1
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