Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10943
Gene Symbol: MSL3
MSL3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 4297
Gene Symbol: KMT2A
KMT2A 		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: 9871
Gene Symbol: SEC24D
SEC24D 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 3192
Gene Symbol: HNRNPU
HNRNPU 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 6326
Gene Symbol: SCN2A
SCN2A 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 92154
Gene Symbol: MTSS2
MTSS2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 113179
Gene Symbol: ADAT3
ADAT3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 23314
Gene Symbol: SATB2
SATB2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 51633
Gene Symbol: OTUD6B
OTUD6B 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 3785
Gene Symbol: KCNQ2
KCNQ2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 9126
Gene Symbol: SMC3
SMC3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 53335
Gene Symbol: BCL11A
BCL11A 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 113178
Gene Symbol: SCAMP4
SCAMP4 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 22907
Gene Symbol: DHX30
DHX30 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 10084
Gene Symbol: PQBP1
PQBP1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 2332
Gene Symbol: FMR1
FMR1 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 26224
Gene Symbol: FBXL3
FBXL3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 1107
Gene Symbol: CHD3
CHD3 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 8208
Gene Symbol: CHAF1B
CHAF1B 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 673
Gene Symbol: BRAF
BRAF 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 547
Gene Symbol: KIF1A
KIF1A 		0.100 GeneticVariation phenotype CLINVAR
Entrez Id: 55768
Gene Symbol: NGLY1
NGLY1 		0.100 GeneticVariation phenotype CLINVAR NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy. 25220016 2015