"3billion"[submitter] AND "LMNA"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 66912	NM_170707.4(LMNA):c.575A>T (p.Asp192Val)	LMNA (D192V +2 more)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy 1A	GLikely pathogenic
Select item 180115	NM_170707.4(LMNA):c.686T>C (p.Ile229Thr)	LMNA (I229T +2 more)	Single nucleotide variant (missense variant)	Familial partial lipodystrophy, Dunnigan type +4 more	GConflicting classifications of pathogenicity
Select item 285938	NM_170707.4(LMNA):c.851T>C (p.Leu284Pro)	LMNA (L284P +2 more)	Single nucleotide variant (missense variant)	Congenital muscular dystrophy due to LMNA mutation +1 more	GPathogenic
Select item 36476	NM_170707.4(LMNA):c.1412G>A (p.Arg471His)	LMNA (R471H +2 more)	Single nucleotide variant (missense variant)	not provided +4 more	GPathogenic/Likely pathogenic
Select item 1526037	NM_170707.4(LMNA):c.1608+2T>A	LMNA	Single nucleotide variant (splice donor variant)	Dilated cardiomyopathy 1A	GLikely pathogenic
Select item 14500	NM_170707.4(LMNA):c.1824C>T (p.Gly608=)	LMNA	Single nucleotide variant (synonymous variant +1 more)	Primary dilated cardiomyopathy +3 more	GPathogenic

ClinVar