List of variants in gene combination LOC126806433, 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)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.6959G>A (p.Arg2320His)	rs374615369	0.00008
NM_001267550.2(TTN):c.6953G>A (p.Arg2318His)	rs761566436	0.00003
NM_001267550.2(TTN):c.6995A>G (p.Asp2332Gly)	rs749655939	0.00003
NM_001267550.2(TTN):c.6895T>C (p.Trp2299Arg)	rs145585333	0.00002
NM_001267550.2(TTN):c.6923C>A (p.Ser2308Tyr)	rs577966527	0.00002
NM_001267550.2(TTN):c.7399A>G (p.Lys2467Glu)	rs1362423521	0.00001
NM_001267550.2(TTN):c.7208T>C (p.Ile2403Thr)	rs760895168

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