ClinVar Miner

List of variants reported as uncertain significance 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.1671G>C (p.Leu557Phe)
NM_018023.5(YEATS2):c.4087G>A (p.Ala1363Thr)	rs2108544825
NM_018023.5(YEATS2):c.444C>G (p.Asp148Glu)	rs1716550954

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