List of variants in gene combination LOC129935183, TTN reported as likely benign for 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.105940G>A (p.Ala35314Thr)	rs377171054	0.00011
NM_001267550.2(TTN):c.105876G>A (p.Leu35292=)	rs372521529	0.00010
NM_001267550.2(TTN):c.105787_105788delinsTT (p.Ala35263Phe)	rs794729250
NM_001267550.2(TTN):c.105897G>C (p.Glu35299Asp)	rs886055219

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