List of variants in gene combination LOC126806422, 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp)	rs201043950	0.00110
NM_001267550.2(TTN):c.70111C>T (p.Arg23371Cys)	rs56141309	0.00001
NM_001267550.2(TTN):c.69837T>A (p.His23279Gln)	rs752879532
NM_001267550.2(TTN):c.70112G>C (p.Arg23371Pro)	rs767208489
NM_001267550.2(TTN):c.70597C>T (p.Pro23533Ser)	rs886055250

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