"Clinical Genetics, Academic Medical Center"[submitter] AND "LOC110121 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 227494	NM_007078.3(LDB3):c.689+3861C>T	LDB3, LOC110121486	Single nucleotide variant (intron variant)	Myofibrillar myopathy 4 +4 more	GConflicting classifications of pathogenicity
Select item 43875	NM_007078.3(LDB3):c.690-4842G>A	LDB3, LOC110121486	Single nucleotide variant (intron variant)	not specified +5 more	GBenign/Likely benign
Select item 414137	NM_007078.3(LDB3):c.690-4837C>T	LDB3, LOC110121486	Single nucleotide variant (intron variant)	Myofibrillar myopathy 4 +1 more	GBenign/Likely benign
Select item 4733	NM_001368067.1(LDB3):c.349G>A (p.Asp117Asn)	LDB3, LOC110121486 (D117N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 43879	NM_001368067.1(LDB3):c.504T>C (p.Asp168=)	LDB3, LOC110121486	Single nucleotide variant (synonymous variant +1 more)	not specified +6 more	GBenign/Likely benign
Select item 43880	NM_001368067.1(LDB3):c.546T>C (p.Ser182=)	LDB3, LOC110121486	Single nucleotide variant (synonymous variant +1 more)	Dilated Cardiomyopathy, Dominant +6 more	GConflicting classifications of pathogenicity
Select item 518922	NM_007078.3(LDB3):c.690-4621A>G	LOC110121486, LDB3	Single nucleotide variant (intron variant)	Myofibrillar myopathy 4 +2 more	GUncertain significance

ClinVar