List of variants in gene combination LOC126806427, TTN reported as likely pathogenic for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J

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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.45156T>A (p.Cys15052Ter)	rs1060500487
NM_001267550.2(TTN):c.45383del (p.Asn15128fs)
NM_001267550.2(TTN):c.45459del (p.Arg15154fs)

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