Gene: ARID1B ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554237050
rs1554237050
ARID1B
G 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs1554237050
rs1554237050
ARID1B
G 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554237658
rs1554237658
ARID1B
T 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554237658
rs1554237658
ARID1B
T 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs1554237848
rs1554237848
ARID1B
A 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs1554237848
rs1554237848
ARID1B
A 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554247637
rs1554247637
ARID1B
G 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs1554247637
rs1554247637
ARID1B
G 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554256703
rs1554256703
ARID1B
T 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554256703
rs1554256703
ARID1B
T 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs758570139
rs758570139
ARID1B
G 0.700 CausalMutation CLINVAR De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia. 27389779

2017
dbSNP: rs758570139
rs758570139
ARID1B
G 0.700 CausalMutation CLINVAR Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice. 28867767

2017
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs1554237050
rs1554237050
ARID1B
G 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs1554237658
rs1554237658
ARID1B
T 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs1554237848
rs1554237848
ARID1B
A 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs1554247637
rs1554247637
ARID1B
G 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs1554256703
rs1554256703
ARID1B
T 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs758570139
rs758570139
ARID1B
G 0.700 CausalMutation CLINVAR Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings. 26395437

2016
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature. 26376624

2015
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR ARID1B-mediated disorders: Mutations and possible mechanisms. 25674384

2015
dbSNP: rs1554237050
rs1554237050
ARID1B
G 0.700 CausalMutation CLINVAR De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature. 26376624

2015
dbSNP: rs1554237050
rs1554237050
ARID1B
G 0.700 CausalMutation CLINVAR ARID1B-mediated disorders: Mutations and possible mechanisms. 25674384

2015