List of variants in gene PRDM16 reported as pathogenic for 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022114.4(PRDM16):c.872C>T (p.Pro291Leu)	rs397514744	0.00003
NM_022114.4(PRDM16):c.2660T>C (p.Leu887Pro)	rs202115331

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