ClinVar Miner

List of variants reported as pathogenic for Laminopathy

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_170707.4(LMNA):c.1045C>T (p.Arg349Trp)	rs267607555	0.00001
NM_170707.4(LMNA):c.1445G>A (p.Arg482Gln)	rs11575937	0.00001
NM_170707.4(LMNA):c.1621C>T (p.Arg541Cys)	rs56984562

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