List of variants in gene combination LOC126806423, TTN reported as likely pathogenic 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67636+2T>C	rs1575872984	0.00001
NM_001267550.2(TTN):c.67421del (p.Lys22474fs)	rs794729332
NM_001267550.2(TTN):c.67906_67909dup (p.Ser22637fs)	rs2468869047

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