List of variants in gene combination LOC101927055, 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.4057_4058del (p.Val1353fs)
NM_001267550.2(TTN):c.4293del (p.Met1432fs)
NM_001267550.2(TTN):c.4592_4596del (p.Val1531fs)	rs1131691910

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