List of variants in gene TTN reported as likely benign for Dilated Cardiomyopathy, Dominant

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_133379.5(TTN):c.16001C>T (p.Pro5334Leu)	rs151253841	0.00010
NM_001267550.2(TTN):c.*99dup	rs11424072
NM_001267550.2(TTN):c.26762-39TTTGT[7]	rs71393436
NM_001267550.2(TTN):c.26762-39TTTGT[8]	rs71393436
NM_133378.4(TTN):c.26780-19dup	rs397517532

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