ClinVar Miner

List of variants reported as uncertain significance for Epilepsy, familial adult myoclonic, 6

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_014494.4(TNRC6A):c.136AAG[1] (p.Lys47del)	rs2151408186
NM_014494.4(TNRC6A):c.3838-10G>T	rs760665329
NM_014494.4(TNRC6A):c.5779A>G (p.Ser1927Gly)

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