ClinVar Miner

List of variants reported as uncertain significance for Epilepsy, idiopathic generalized, susceptibility to, 9; Episodic ataxia type 5 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000726.5(CACNB4):c.44C>G (p.Pro15Arg)	rs200662010	0.00201
NM_000726.5(CACNB4):c.5C>T (p.Ser2Phe)	rs200092211	0.00091
NM_000726.5(CACNB4):c.91A>C (p.Ser31Arg)	rs773391545	0.00009

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