List of variants reported as benign for Epilepsy, childhood absence, susceptibility to, 6 by Genome Diagnostics Laboratory, University Medical Center Utrecht

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_021098.3(CACNA1H):c.6417T>C (p.Asp2139=)	rs4247094	0.85388
NM_021098.3(CACNA1H):c.3957T>C (p.Asp1319=)	rs8063574	0.85136
NM_021098.3(CACNA1H):c.6230G>A (p.Arg2077His)	rs1054645	0.64981
NM_021098.3(CACNA1H):c.5947T>C (p.Leu1983=)	rs2738893	0.63925
NM_021098.3(CACNA1H):c.5493C>T (p.Tyr1831=)	rs60218977	0.00542

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