ClinVar Miner

List of variants reported as likely benign for Epilepsy, familial adult myoclonic, 4

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_018023.5(YEATS2):c.1601C>A (p.Thr534Lys)	rs34759333	0.01226
NM_018023.5(YEATS2):c.3764C>T (p.Thr1255Ile)
NM_018023.5(YEATS2):c.3960C>G (p.Phe1320Leu)

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