List of variants in gene LOC126806428, 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_001267550.2(TTN):c.21163G>T (p.Gly7055Trp)	rs375219301	0.00003
NM_001267550.2(TTN):c.20869A>T (p.Met6957Leu)	rs375262781	0.00001
NM_001267550.2(TTN):c.20873C>T (p.Thr6958Met)	rs371824963	0.00001
NM_001267550.2(TTN):c.20891C>T (p.Thr6964Met)	rs765257439	0.00001
NM_001267550.2(TTN):c.20986T>C (p.Phe6996Leu)	rs753725329	0.00001
NM_001267550.2(TTN):c.21118C>T (p.Arg7040Ter)	rs576359448	0.00001
NM_001267550.2(TTN):c.21143G>A (p.Arg7048Gln)	rs148072021	0.00001
NM_001267550.2(TTN):c.21172G>C (p.Gly7058Arg)	rs786205401	0.00001
NM_001267550.2(TTN):c.21227C>T (p.Ala7076Val)	rs374625641	0.00001
NM_001267550.2(TTN):c.21246C>T (p.Thr7082=)	rs1553913320
NM_001267550.2(TTN):c.21292G>A (p.Val7098Ile)	rs878978917

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