List of variants in gene combination LOC126806424, 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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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.59489A>G (p.Lys19830Arg)	rs764259290	0.00011
NM_001267550.2(TTN):c.59729C>T (p.Thr19910Ile)	rs369476725	0.00010
NM_001267550.2(TTN):c.59474G>C (p.Arg19825Thr)	rs376465623	0.00006
NM_001267550.2(TTN):c.59813C>T (p.Ala19938Val)	rs1187337182	0.00005
NM_001267550.2(TTN):c.59926C>T (p.His19976Tyr)	rs727503588	0.00005
NM_001267550.2(TTN):c.59711A>G (p.Asp19904Gly)	rs1016296280	0.00001
NM_001267550.2(TTN):c.59912C>T (p.Ala19971Val)	rs886055258	0.00001
NM_001267550.2(TTN):c.59570T>C (p.Leu19857Ser)	rs547180437
NM_001267550.2(TTN):c.59707G>A (p.Asp19903Asn)	rs374163882

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