List of variants in gene LDB3 reported as uncertain significance for Primary dilated cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_007078.3(LDB3):c.794G>A (p.Arg265His)	rs45458895	0.00011
NM_007078.3(LDB3):c.1703G>A (p.Arg568His)	rs769156627	0.00002
NM_007078.3(LDB3):c.91C>T (p.Arg31Trp)	rs367792378	0.00001

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