Variant: rs786200963 

    present in Gene: CACNA1A
    present in Chromosome: 19
    Position on Chromosome: 13371683
    Alleles of this Variant: C/T

rs786200963 in CACNA1A gene and Attention deficit hyperactivity disorder PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs786200963 in CACNA1A gene and Episodic Ataxia PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs786200963 in CACNA1A gene and Episodic ataxia type 2 (disorder) PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs786200963 in CACNA1A gene and Febrile Convulsions PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs786200963 in CACNA1A gene and Learning difficulties PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs786200963 in CACNA1A gene and Mild Mental Retardation PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.