ClinVar Miner

List of variants reported as uncertain significance for Epilepsy, familial adult myoclonic, 1 by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_207506.3(SAMD12):c.362G>T (p.Arg121Leu)

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