ClinVar Miner

List of variants studied for Dilated cardiomyopathy 1A; Charcot-Marie-Tooth disease type 2B1; Emery-Dreifuss muscular dystrophy 2, autosomal dominant; Hutchinson-Gilford syndrome; Congenital muscular dystrophy due to LMNA mutation; Emery-Dreifuss muscular dystrophy 3, autosomal recessive

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1045C>T (p.Arg349Trp)	rs267607555	0.00001

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