"Institute of Human Genetics, University of Wuerzburg"[submitter] AND - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 915503	NM_007078.3(LDB3):c.1299T>C (p.Pro433=)	LDB3	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GBenign
Select item 915504	NM_007078.3(LDB3):c.1300G>C (p.Ala434Pro)	LDB3 (A324P +4 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GBenign/Likely benign
Select item 1329289	NM_007078.3(LDB3):c.1305T>C (p.Pro435=)	LDB3	Single nucleotide variant (synonymous variant)	Cardiomyopathy	GBenign
Select item 1299814	NM_007078.3(LDB3):c.1318T>C (p.Ser440Pro)	LDB3 (S330P +4 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 3255551	NM_007078.3(LDB3):c.1324G>C (p.Ala442Pro)	LDB3 (A332P +4 more)	Single nucleotide variant (missense variant)	Hypertrophic cardiomyopathy 2	Gnot provided

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