List of variants studied for laminopathy by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_138711.6(PPARG):c.362A>G (p.Tyr121Cys)	rs1354592503	0.00001
NM_170707.4(LMNA):c.1003C>T (p.Arg335Trp)	rs386134243	0.00001
NM_170707.4(LMNA):c.1303C>T (p.Arg435Cys)	rs150840924	0.00001
NM_170707.4(LMNA):c.1445G>A (p.Arg482Gln)	rs11575937	0.00001
NM_170707.4(LMNA):c.646C>T (p.Arg216Cys)	rs794728591	0.00001
NM_170707.2(LMNA):c.(?_1)_(356_?)del
NM_170707.4(LMNA):c.1110C>G (p.Asp370Glu)	rs876657649
NM_170707.4(LMNA):c.1824C>T (p.Gly608=)	rs58596362
NM_170707.4(LMNA):c.745C>G (p.Arg249Gly)	rs121912496

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