List of variants in gene combination LOC126806422, TTN reported as benign 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)
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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69585C>T (p.Ser23195=)	rs67041405	0.01183
NM_001267550.2(TTN):c.69740C>T (p.Pro23247Leu)	rs115658240	0.00835
NM_001267550.2(TTN):c.69676A>G (p.Ser23226Gly)	rs72646885	0.00553
NM_001267550.2(TTN):c.69716-5C>G	rs72646886	0.00290
NM_001267550.2(TTN):c.69821G>A (p.Gly23274Asp)	rs201043950	0.00110
NM_001267550.2(TTN):c.70250T>C (p.Ile23417Thr)	rs201836227	0.00086
NM_001267550.2(TTN):c.70491C>T (p.Thr23497=)	rs372382315	0.00031
NM_001267550.2(TTN):c.69864A>G (p.Ile23288Met)	rs368867993	0.00026
NM_001267550.2(TTN):c.70492G>A (p.Gly23498Ser)	rs370771532	0.00026
NM_001267550.2(TTN):c.70651C>T (p.Leu23551=)	rs72646889	0.00011
NM_001267550.2(TTN):c.70131A>G (p.Thr23377=)	rs369503828	0.00010
NM_001267550.2(TTN):c.70506G>T (p.Gly23502=)	rs181702963	0.00007
NM_001267550.2(TTN):c.70305G>A (p.Thr23435=)	rs397517684	0.00006
NM_001267550.2(TTN):c.70380G>A (p.Leu23460=)	rs185660043	0.00006
NM_001267550.2(TTN):c.70579G>A (p.Val23527Ile)	rs542004766

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