List of variants in gene LOC126806431, 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.17129G>A (p.Arg5710Gln)	rs200018866	0.00022
NM_001267550.2(TTN):c.16825G>A (p.Glu5609Lys)	rs374682077	0.00009
NM_001267550.2(TTN):c.17437T>A (p.Cys5813Ser)	rs368692616	0.00009
NM_001267550.2(TTN):c.17375T>C (p.Ile5792Thr)	rs1225094303	0.00001
NM_001267550.2(TTN):c.17376T>G (p.Ile5792Met)	rs1041967765	0.00001
NM_001267550.2(TTN):c.17645T>C (p.Ile5882Thr)	rs763665430	0.00001
NM_001267550.2(TTN):c.17669G>C (p.Ser5890Thr)	rs775293848	0.00001
NM_001267550.2(TTN):c.17357G>T (p.Ser5786Ile)	rs1553924253
NM_001267550.2(TTN):c.17558C>T (p.Thr5853Ile)	rs2154308873

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