List of variants in gene combination LOC129935183, 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.105737C>T (p.Ala35246Val)	rs370476812
NM_001267550.2(TTN):c.105772C>A (p.Pro35258Thr)	rs886055220
NM_001267550.2(TTN):c.105897G>C (p.Glu35299Asp)	rs886055219

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