List of variants in gene combination LOC101927055, 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.4031A>G (p.Asp1344Gly)	rs1203373476	0.00001
NM_001267550.2(TTN):c.4874C>G (p.Ser1625Cys)	rs185789611	0.00001
NM_001267550.2(TTN):c.4319G>T (p.Gly1440Val)	rs150579194
NM_001267550.2(TTN):c.4506C>T (p.Thr1502=)	rs185660585

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