List of variants in gene LOC126806430, TTN studied 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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18893T>C (p.Ile6298Thr)	rs375571785	0.00006
NM_001267550.2(TTN):c.18374T>C (p.Phe6125Ser)	rs375003845	0.00002
NM_001267550.2(TTN):c.18150A>G (p.Lys6050=)	rs991259759	0.00001
NM_001267550.2(TTN):c.18589G>C (p.Glu6197Gln)	rs753281535	0.00001
NM_001267550.2(TTN):c.18673A>G (p.Thr6225Ala)	rs794727818

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