List of variants in gene combination LOC126806426, TTN reported as uncertain significance for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9

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Minimum conflict level: Report conflict between different conditions
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.49000G>A (p.Val16334Met)	rs541384076	0.00008
NM_001267550.2(TTN):c.48751G>A (p.Asp16251Asn)	rs199954570	0.00006
NM_001267550.2(TTN):c.48838G>A (p.Ala16280Thr)	rs372911542	0.00006

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