C0796031[trait identifier] AND "OMIM"[submitter] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 14506	NM_170707.4(LMNA):c.169G>C (p.Ala57Pro)	LMNA (A57P)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome	GPathogenic
Select item 18457	NM_170707.4(LMNA):c.176T>G (p.Leu59Arg)	LMNA (L59R)	Single nucleotide variant (missense variant)	Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome	GPathogenic
Select item 36473	NM_170707.4(LMNA):c.1003C>T (p.Arg335Trp)	LMNA (R335W +2 more)	Single nucleotide variant (missense variant)	Left ventricular noncompaction +20 more	GPathogenic/Likely pathogenic
Select item 14489	NM_170707.4(LMNA):c.1444C>T (p.Arg482Trp)	LMNA (R482W +2 more)	Single nucleotide variant (missense variant)	Familial partial lipodystrophy, Dunnigan type +16 more	GPathogenic
Select item 14486	NM_170707.4(LMNA):c.1445G>A (p.Arg482Gln)	LMNA (R482Q +2 more)	Single nucleotide variant (missense variant)	Laminopathy +17 more	GConflicting classifications of pathogenicity
Select item 14527	NM_170707.4(LMNA):c.1930C>T (p.Arg644Cys)	LMNA (R644C +6 more)	Single nucleotide variant (missense variant +1 more)	not provided +18 more	GConflicting classifications of pathogenicity

ClinVar