List of variants in gene LOC126806427, 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.45128G>A (p.Ser15043Asn)	rs376144178	0.00004
NM_001267550.2(TTN):c.45199G>A (p.Asp15067Asn)	rs370904881	0.00004
NM_001267550.2(TTN):c.44916T>A (p.Val14972=)	rs373390402	0.00003
NM_001267550.2(TTN):c.45001A>C (p.Asn15001His)	rs373109469

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