Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 501
Gene Symbol: ALDH7A1
ALDH7A1
0.100 Biomarker phenotype HPO
Entrez Id: 79868
Gene Symbol: ALG13
ALG13
0.100 Biomarker phenotype HPO
Entrez Id: 288
Gene Symbol: ANK3
ANK3
0.100 Biomarker phenotype HPO
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11
0.100 CausalMutation phenotype CLINVAR
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11
0.100 Biomarker phenotype HPO
Entrez Id: 118429
Gene Symbol: ANTXR2
ANTXR2
0.100 CausalMutation phenotype CLINVAR
Entrez Id: 8120
Gene Symbol: AP3B2
AP3B2
0.100 Biomarker phenotype HPO
Entrez Id: 10717
Gene Symbol: AP4B1
AP4B1
0.100 Biomarker phenotype HPO
Entrez Id: 375
Gene Symbol: ARF1
ARF1
0.100 Biomarker phenotype HPO
Entrez Id: 9411
Gene Symbol: ARHGAP29
ARHGAP29
0.100 Biomarker phenotype HPO
Entrez Id: 9459
Gene Symbol: ARHGEF6
ARHGEF6
0.100 Biomarker phenotype HPO
Entrez Id: 8289
Gene Symbol: ARID1A
ARID1A
0.100 Biomarker phenotype HPO
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B
0.100 CausalMutation phenotype CLINVAR Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. 26350204 2015
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B
0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B
0.100 CausalMutation phenotype CLINVAR Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome. 22426309 2012
Entrez Id: 196528
Gene Symbol: ARID2
ARID2
0.100 CausalMutation phenotype CLINVAR
Entrez Id: 196528
Gene Symbol: ARID2
ARID2
0.100 Biomarker phenotype HPO
Entrez Id: 55130
Gene Symbol: ARMC4
ARMC4
0.100 Biomarker phenotype HPO
Entrez Id: 80210
Gene Symbol: ARMC9
ARMC9
0.100 Biomarker phenotype HPO
Entrez Id: 64801
Gene Symbol: ARV1
ARV1
0.100 Biomarker phenotype HPO
Entrez Id: 170302
Gene Symbol: ARX
ARX
0.100 Biomarker phenotype HPO
Entrez Id: 443
Gene Symbol: ASPA
ASPA
0.100 Biomarker phenotype HPO
Entrez Id: 259266
Gene Symbol: ASPM
ASPM
0.100 Biomarker phenotype HPO
Entrez Id: 171023
Gene Symbol: ASXL1
ASXL1
0.100 CausalMutation phenotype CLINVAR
Entrez Id: 55252
Gene Symbol: ASXL2
ASXL2
0.100 Biomarker phenotype HPO