rs11967485
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Calcium measurement
|
A |
0.800 |
GeneticVariation |
GWASDB |
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
|
24068962 |
2013 |
rs11967485
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Calcium measurement
|
A |
0.800 |
GeneticVariation |
GWASCAT |
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
|
24068962 |
2013 |
rs17322427
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Red Blood Cell Count measurement
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs112140754
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Diastolic blood pressure
|
|
0.700 |
GeneticVariation |
GWASCAT |
A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.
|
29455858 |
2018 |
rs287879
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Intelligence
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.
|
29942086 |
2018 |
rs1554226131
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Muscle hypotonia
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554226131
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Muscle hypotonia
|
CA |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554226131
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554226131
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
CA |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554231814
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Multiple congenital anomalies
|
G |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554231814
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Multiple congenital anomalies
|
G |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554234424
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Multiple congenital anomalies
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554234424
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Multiple congenital anomalies
|
A |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554234424
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554234424
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554235792
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
G |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554235792
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
G |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554236054
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
AG |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554236054
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Movement Disorders
|
AG |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554236054
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Movement Disorders
|
AG |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554236054
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Dysmorphic features
|
AG |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554236054
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Multiple congenital anomalies
|
AG |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |
rs1554236054
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Multiple congenital anomalies
|
AG |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554237050
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Muscle hypotonia
|
G |
0.700 |
CausalMutation |
CLINVAR |
Arid1b Haploinsufficiency Causes Abnormal Brain Gene Expression and Autism-Related Behaviors in Mice.
|
28867767 |
2017 |
rs1554237050
|
Entrez Id: |
57492 |
Gene Symbol: |
ARID1B |
ARID1B
|
Muscle hypotonia
|
G |
0.700 |
CausalMutation |
CLINVAR |
De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia.
|
27389779 |
2017 |