List of variants reported as benign for Epilepsy, progressive myoclonic 7

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Total variants: 8

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HGVS	dbSNP
NM_001112741.1(KCNC1):c.1017A>C (p.Arg339=)	rs137989254
NM_001112741.1(KCNC1):c.1236C>T (p.Ser412=)	rs73424033
NM_001112741.1(KCNC1):c.1287C>A (p.Ala429=)	rs139804857
NM_001112741.1(KCNC1):c.72G>A (p.Ser24=)	rs76929858
NM_001112741.1(KCNC1):c.744C>T (p.Ile248=)	rs2229007
NM_001112741.1(KCNC1):c.933C>T (p.Arg311=)	rs76882721
NM_001112741.2(KCNC1):c.1451A>G (p.Gln484Arg)	rs770586397
NM_001112741.2(KCNC1):c.717C>T (p.Ala239=)	rs143670270

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