List of variants in gene combination LOC126806420, 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.100163G>A (p.Ser33388Asn)	rs745406517	0.00004
NM_001267550.2(TTN):c.99752A>G (p.Tyr33251Cys)	rs377456237	0.00003
NM_001267550.2(TTN):c.100117G>A (p.Gly33373Ser)	rs55880786	0.00002
NM_001267550.2(TTN):c.100244C>T (p.Pro33415Leu)	rs72648282
NM_001267550.2(TTN):c.99814C>T (p.Leu33272Phe)	rs397517780

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