List of variants in gene combination LOC126806430, 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18646G>A (p.Val6216Met)	rs369242073	0.00003
NM_001267550.2(TTN):c.18427G>A (p.Gly6143Arg)	rs757453585	0.00002
NM_001267550.2(TTN):c.18364T>C (p.Ser6122Pro)	rs2080087332
NM_001267550.2(TTN):c.18472G>A (p.Asp6158Asn)	rs2080068286
NM_001267550.2(TTN):c.18493A>G (p.Ile6165Val)	rs886055296
NM_001267550.2(TTN):c.18690C>T (p.Val6230=)	rs754536598

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