Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs926027867
rs926027867
CAMK2A
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability. 29100089

2017
dbSNP: rs886041521
rs886041521
ANKRD11
CUI: C1843367
Disease: Poor school performance
Poor school performance 		CT 0.700 CausalMutation CLINVAR

dbSNP: rs886041239
rs886041239
SMC3
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs886041125
rs886041125
ANKRD11
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 GeneticVariation CLINVAR

dbSNP: rs886041125
rs886041125
ANKRD11
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 CausalMutation CLINVAR

dbSNP: rs886041090
rs886041090
BRPF1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041089
rs886041089
FMR1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041088
rs886041088
FMR1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 CausalMutation CLINVAR

dbSNP: rs886040960
rs886040960
KMT2D
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886040857
rs886040857
EIF2S3
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886039396
rs886039396
KCNB1 ; LOC105372649
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR

dbSNP: rs879255590
rs879255590
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255586
rs879255586
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		CA 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255585
rs879255585
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255584
rs879255584
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255583
rs879255583
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255582
rs879255582
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255581
rs879255581
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		C 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879255580
rs879255580
CLCN4
CUI: C1843367
Disease: Poor school performance
Poor school performance 		G 0.700 CausalMutation CLINVAR De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females. 27550844

2018
dbSNP: rs879253753
rs879253753
ANKRD11
CUI: C1843367
Disease: Poor school performance
Poor school performance 		CT 0.700 CausalMutation CLINVAR

dbSNP: rs879253748
rs879253748
GABRA1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 CausalMutation CLINVAR

dbSNP: rs878853264
rs878853264
ARHGAP4 ; NAA10
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs876661308
rs876661308
MEF2C
CUI: C1843367
Disease: Poor school performance
Poor school performance 		A 0.700 CausalMutation CLINVAR MEF2C haploinsufficiency syndrome: Report of a new MEF2C mutation and review. 27255693

2016
dbSNP: rs875989808
rs875989808
SYNGAP1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 GeneticVariation CLINVAR

dbSNP: rs875989807
rs875989807
EP300 ; EP300-AS1
CUI: C1843367
Disease: Poor school performance
Poor school performance 		T 0.700 GeneticVariation CLINVAR