List of variants in gene combination LOC126806423, TTN reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67643C>T (p.Pro22548Leu)	rs763002536	0.00004
NM_001267550.2(TTN):c.68285T>C (p.Leu22762Pro)	rs1359881893	0.00001
NM_001267550.2(TTN):c.67856G>A (p.Gly22619Glu)	rs886055252

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