List of variants reported as uncertain significance for Epilepsy, familial adult myoclonic, 5 by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_005076.5(CNTN2):c.1460C>T (p.Thr487Ile)	rs116647440	0.00047
NM_005076.5(CNTN2):c.214C>T (p.Arg72Trp)	rs149564430	0.00034
NM_005076.5(CNTN2):c.1216G>A (p.Ala406Thr)	rs752262787	0.00007
NM_005076.5(CNTN2):c.1975+10A>G	rs773175563

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