List of variants in gene combination LOC126806421, 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96268C>T (p.Gln32090Ter)	rs876657671
NM_001267550.2(TTN):c.96460dup (p.Thr32154fs)	rs869312084
NM_001267550.2(TTN):c.96598_96599del (p.Ser32200fs)
NM_001267550.2(TTN):c.96870_96871del (p.Glu32290fs)	rs1695435412

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