List of variants in gene combination LOC126806423, TTN reported as benign for Myopathy, myofibrillar, 9, with early respiratory failure

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67637-17T>C	rs2288571	0.24363
NM_001267550.2(TTN):c.68217T>C (p.His22739=)	rs10497517	0.09829
NM_001267550.2(TTN):c.67635T>C (p.Val22545=)	rs2288570	0.02106
NM_001267550.2(TTN):c.68079G>A (p.Thr22693=)	rs11904444	0.00481
NM_001267550.2(TTN):c.67542T>G (p.Thr22514=)	rs72646876	0.00048
NM_001267550.2(TTN):c.67833C>T (p.Tyr22611=)	rs375538420	0.00027
NM_001267550.2(TTN):c.68082C>T (p.Cys22694=)	rs79406408	0.00024
NM_001267550.2(TTN):c.68208T>A (p.Val22736=)	rs727503575	0.00006
NM_001267550.2(TTN):c.67809G>A (p.Ala22603=)	rs548223512	0.00002
NM_001267550.2(TTN):c.67960G>C (p.Asp22654His)	rs144295295	0.00001
NM_001267550.2(TTN):c.68160C>T (p.Ala22720=)	rs397517673	0.00001

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