Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 60
Gene Symbol: ACTB
ACTB 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 51412
Gene Symbol: ACTL6B
ACTL6B 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 113179
Gene Symbol: ADAT3
ADAT3 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 113179
Gene Symbol: ADAT3
ADAT3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 9289
Gene Symbol: ADGRG1
ADGRG1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 27245
Gene Symbol: AHDC1
AHDC1 		0.100 CausalMutation phenotype CLINVAR De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea. 24791903 2014
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 29123
Gene Symbol: ANKRD11
ANKRD11 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 393
Gene Symbol: ARHGAP4
ARHGAP4 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 393
Gene Symbol: ARHGAP4
ARHGAP4 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 57492
Gene Symbol: ARID1B
ARID1B 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 9070
Gene Symbol: ASH2L
ASH2L 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 259266
Gene Symbol: ASPM
ASPM 		0.100 GeneticVariation phenotype CLINVAR ASPM is a major determinant of cerebral cortical size. 12355089 2002
Entrez Id: 259266
Gene Symbol: ASPM
ASPM 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 259266
Gene Symbol: ASPM
ASPM 		0.100 GeneticVariation phenotype CLINVAR Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations. 19770472 2009
Entrez Id: 492
Gene Symbol: ATP2B3
ATP2B3 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 526
Gene Symbol: ATP6V1B2
ATP6V1B2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 546
Gene Symbol: ATRX
ATRX 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 582
Gene Symbol: BBS1
BBS1 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 79738
Gene Symbol: BBS10
BBS10 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 166379
Gene Symbol: BBS12
BBS12 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 583
Gene Symbol: BBS2
BBS2 		0.100 CausalMutation phenotype CLINVAR
Entrez Id: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype CLINVAR