List of variants in gene combination LOC126806426, TTN reported as likely pathogenic for Primary dilated cardiomyopathy

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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_001267550.2(TTN):c.48761-1G>C	rs876657665
NM_001267550.2(TTN):c.48836del (p.Pro16279fs)
NM_001267550.2(TTN):c.48863del (p.Pro16288fs)	rs794729320

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