ClinVar Miner

List of variants reported as likely benign for Epilepsy, familial adult myoclonic, 5 by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005076.5(CNTN2):c.391+12G>A	rs16855012	0.01337
NM_005076.5(CNTN2):c.1287C>T (p.Pro429=)	rs145911280	0.00202
NM_005076.5(CNTN2):c.2844+11A>C	rs377297728	0.00019

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