List of variants in gene LOC126806432, 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_133379.5(TTN):c.14806A>T (p.Thr4936Ser)	rs72648909	0.00042
NM_133379.5(TTN):c.14240A>T (p.Asp4747Val)	rs149586047	0.00031
NM_133379.5(TTN):c.15122C>G (p.Thr5041Arg)	rs148791107	0.00016
NM_133379.5(TTN):c.13984A>G (p.Ile4662Val)	rs374783099	0.00006
NM_133379.5(TTN):c.14321A>G (p.Lys4774Arg)	rs768589711	0.00006
NM_133379.5(TTN):c.13951A>G (p.Ser4651Gly)	rs190193836	0.00004
NM_133379.5(TTN):c.14113C>T (p.Arg4705Ter)	rs755956493	0.00003
NM_133379.5(TTN):c.14790C>G (p.Val4930=)	rs370038956	0.00003
NM_133379.5(TTN):c.14911A>G (p.Ile4971Val)	rs727504687	0.00003
NM_133379.5(TTN):c.14062G>A (p.Val4688Met)	rs1476964512	0.00002
NM_133379.5(TTN):c.14139C>T (p.Asp4713=)	rs371388583	0.00001

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