ClinVar Miner

List of variants reported as likely pathogenic for dilated cardiomyopathy 1D by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001276345.2(TNNT2):c.506G>A (p.Arg169Gln)	rs45501500
NM_001276345.2(TNNT2):c.616C>T (p.Arg206Trp)	rs730881106

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