List of variants reported as risk factor for Epilepsy, childhood absence, susceptibility to, 6 by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_021098.3(CACNA1H):c.2491G>A (p.Val831Met)	rs119454949	0.00002
NM_021098.3(CACNA1H):c.844G>A (p.Glu282Lys)	rs119454948	0.00001
NM_021098.2(CACNA1H):c.[2318G>A;2362C>T]
NM_021098.3(CACNA1H):c.483C>A (p.Phe161Leu)	rs119454947

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