List of variants in gene combination LOC126806425, 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.53002+10G>A	rs370352450	0.00006
NM_001267550.2(TTN):c.52526G>A (p.Arg17509His)	rs886055267	0.00001
NM_001267550.2(TTN):c.52948G>A (p.Ala17650Thr)	rs535008556	0.00001
NM_001267550.2(TTN):c.52709C>T (p.Pro17570Leu)	rs2055350149
NM_001267550.2(TTN):c.53100T>C (p.Pro17700=)	rs373140387
NM_001267550.2(TTN):c.53236G>A (p.Ala17746Thr)	rs886055266
NM_001267550.2(TTN):c.53322T>G (p.Val17774=)	rs886055265

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