"Baylor Genetics"[submitter] AND "LMNB2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 772460	NM_032737.4(LMNB2):c.1796G>A (p.Gly599Asp)	LMNB2 (G599D)	Single nucleotide variant (missense variant)	Progressive myoclonic epilepsy type 9 +1 more	GConflicting classifications of pathogenicity
Select item 1034159	NM_032737.4(LMNB2):c.891C>G (p.Asp297Glu)	LMNB2 (D297E)	Single nucleotide variant (missense variant)	Progressive myoclonic epilepsy type 9	GUncertain significance
Select item 2582532	NM_032737.4(LMNB2):c.859G>A (p.Asp287Asn)	LMNB2 (D287N)	Single nucleotide variant (missense variant)	Microcephaly 27, primary, autosomal dominant	GUncertain significance
Select item 1034158	NM_032737.4(LMNB2):c.572A>G (p.His191Arg)	LMNB2 (H191R)	Single nucleotide variant (missense variant)	Progressive myoclonic epilepsy type 9 +1 more	GUncertain significance
Select item 652532	NM_032737.4(LMNB2):c.281C>T (p.Ala94Val)	LMNB2 (A94V)	Single nucleotide variant (missense variant)	Lipodystrophy, partial, acquired, susceptibility to +1 more	GConflicting classifications of pathogenicity
Select item 445837	NM_032737.4(LMNB2):c.265-19C>T	LMNB2	Single nucleotide variant (intron variant)	Lipodystrophy, partial, acquired, susceptibility to +2 more	GConflicting classifications of pathogenicity

ClinVar