List of variants reported as uncertain significance for Episodic ataxia type 2; Spinocerebellar ataxia type 6; Migraine, familial hemiplegic, 1; Developmental and epileptic encephalopathy, 42 by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127222.2(CACNA1A):c.3227C>T (p.Ala1076Val)	rs199512932	0.00024
NM_001127222.2(CACNA1A):c.2088G>A (p.Leu696=)	rs908321451
NM_001127222.2(CACNA1A):c.3085A>G (p.Arg1029Gly)	rs1321119725
NM_001127222.2(CACNA1A):c.6271G>A (p.Ala2091Thr)	rs371172398
NM_001127222.2(CACNA1A):c.7266_7271del (p.Ser2423_Gly2424del)	rs775428832

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