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 The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554234424
rs1554234424
ARID1B
A 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554235792
rs1554235792
ARID1B
G 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554236054
rs1554236054
ARID1B
AG 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554237658
rs1554237658
ARID1B
T 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554237848
rs1554237848
ARID1B
A 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554247637
rs1554247637
ARID1B
G 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554256703
rs1554256703
ARID1B
T 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs201653711
rs201653711
ARID1B
T 0.700 GeneticVariation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs758570139
rs758570139
ARID1B
G 0.700 CausalMutation CLINVAR The Coffin-Siris syndrome: report of a family and further delineation. 6499251

1984
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554234424
rs1554234424
ARID1B
A 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554235792
rs1554235792
ARID1B
G 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554236054
rs1554236054
ARID1B
AG 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554237658
rs1554237658
ARID1B
T 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554237848
rs1554237848
ARID1B
A 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554247637
rs1554247637
ARID1B
G 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554256703
rs1554256703
ARID1B
T 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs201653711
rs201653711
ARID1B
T 0.700 GeneticVariation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs758570139
rs758570139
ARID1B
G 0.700 CausalMutation CLINVAR Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study. 11170086

2001
dbSNP: rs1554226131
rs1554226131
ARID1B
CA 0.700 CausalMutation CLINVAR Autosomal dominant syndrome resembling Coffin-Siris syndrome. 16691594

2006
dbSNP: rs1554234424
rs1554234424
ARID1B
A 0.700 CausalMutation CLINVAR Autosomal dominant syndrome resembling Coffin-Siris syndrome. 16691594

2006
dbSNP: rs1554235792
rs1554235792
ARID1B
G 0.700 CausalMutation CLINVAR Autosomal dominant syndrome resembling Coffin-Siris syndrome. 16691594

2006
dbSNP: rs1554236054
rs1554236054
ARID1B
AG 0.700 CausalMutation CLINVAR Autosomal dominant syndrome resembling Coffin-Siris syndrome. 16691594

2006
dbSNP: rs1554237658
rs1554237658
ARID1B
T 0.700 CausalMutation CLINVAR Autosomal dominant syndrome resembling Coffin-Siris syndrome. 16691594

2006