List of variants in gene LOC126806422, 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69740C>T (p.Pro23247Leu)	rs115658240	0.00835
NM_001267550.2(TTN):c.70380G>A (p.Leu23460=)	rs185660043	0.00006
NM_001267550.2(TTN):c.70288G>A (p.Val23430Ile)	rs549709481	0.00004
NM_001267550.2(TTN):c.70570A>G (p.Thr23524Ala)	rs369526268	0.00004
NM_001267550.2(TTN):c.69959A>G (p.Asn23320Ser)	rs756468956	0.00001
NM_001267550.2(TTN):c.70006G>A (p.Val23336Ile)	rs781015638	0.00001
NM_001267550.2(TTN):c.70166C>G (p.Ala23389Gly)	rs1194442496	0.00001
NM_001267550.2(TTN):c.70181C>T (p.Thr23394Met)	rs397517683	0.00001
NM_001267550.2(TTN):c.70243A>C (p.Met23415Leu)	rs200029470	0.00001
NM_001267550.2(TTN):c.70391G>T (p.Gly23464Val)	rs549938348	0.00001
NM_001267550.2(TTN):c.70112G>C (p.Arg23371Pro)	rs767208489
NM_001267550.2(TTN):c.70377T>C (p.Pro23459=)	rs768458635

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