List of variants in gene combination LOC126806429, 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)
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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.19996C>T (p.Pro6666Ser)	rs571231816	0.00010
NM_001267550.2(TTN):c.20057G>A (p.Arg6686Gln)	rs202022304	0.00004
NM_001267550.2(TTN):c.20170G>A (p.Val6724Ile)	rs140143513	0.00004
NM_001267550.2(TTN):c.19970G>T (p.Cys6657Phe)	rs776748717	0.00001

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