Gene: ADNP ×
Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889

2017
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children. 28221363

2017
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children. 28221363

2017
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889

2017
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases. 28191889

2017
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR Premature primary tooth eruption in cognitive/motor-delayed ADNP-mutated children. 28221363

2017
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP gene. 27031564

2016
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Comprehensive molecular testing in patients with high functioning autism spectrum disorder. 26845707

2016
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR Comprehensive molecular testing in patients with high functioning autism spectrum disorder. 26845707

2016
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP gene. 27031564

2016
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR Additional data on the clinical phenotype of Helsmoortel-Van der Aa syndrome associated with a novel truncating mutation in ADNP gene. 27031564

2016
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR Comprehensive molecular testing in patients with high functioning autism spectrum disorder. 26845707

2016
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms. 26637798

2015
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms. 26637798

2015
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms. 26637798

2015
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism. 25169753

2014
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. 25057125

2014
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. 24531329

2014
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. 24531329

2014
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. 25057125

2014
dbSNP: rs1555809919
rs1555809919
ADNP
GA 0.700 CausalMutation CLINVAR The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism. 25169753

2014
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. 25057125

2014
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. 24531329

2014
dbSNP: rs587777526
rs587777526
ADNP
C 0.700 GeneticVariation CLINVAR The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism. 25169753

2014
dbSNP: rs1555809836
rs1555809836
ADNP
C 0.700 CausalMutation CLINVAR Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders. 23160955

2012