Variant: rs121909323 

    present in Gene: CACNA1A
    present in Chromosome: 19
    Position on Chromosome: 13277122
    Alleles of this Variant: G/A

rs121909323 in CACNA1A gene and Attention deficit hyperactivity disorder PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs121909323 in CACNA1A gene and Autistic Disorder PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs121909323 in CACNA1A gene and Downbeat nystagmus PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs121909323 in CACNA1A gene and Epileptic encephalopathy PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs121909323 in CACNA1A gene and Episodic Ataxia PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs121909323 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.

rs121909323 in CACNA1A gene and Febrile Convulsions PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.

rs121909323 in CACNA1A gene and Mental impairment PMID 25735478 2015 CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms.