List of variants in gene TTN reported as likely pathogenic for Left ventricular noncompaction 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.107284C>T (p.Arg35762Ter)	rs1477669354	0.00001
NM_001267550.2(TTN):c.103360del (p.Glu34454fs)	rs760768093
NM_001267550.2(TTN):c.58259G>A (p.Trp19420Ter)	rs869025544
NM_001267550.2(TTN):c.63601C>T (p.Arg21201Ter)	rs764243269
NM_001267550.2(TTN):c.66975_66978del (p.Lys22326fs)	rs587782986
NM_001267550.2(TTN):c.70879C>T (p.Gln23627Ter)	rs1575799625

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