List of variants in gene TTN reported as likely benign for Hypertrophic cardiomyopathy 9

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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.25619C>T (p.Ser8540Phe)	rs201523784	0.00045
NM_001267550.2(TTN):c.36045G>A (p.Thr12015=)	rs1209026573	0.00001
NM_001267550.2(TTN):c.101835C>A (p.Ile33945=)

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