List of variants in gene combination LOC126806428, 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.20861C>T (p.Ala6954Val)	rs17355446	0.02915
NM_001267550.2(TTN):c.21106G>A (p.Asp7036Asn)	rs72648962	0.01709
NM_001267550.2(TTN):c.21044C>T (p.Ala7015Val)	rs72648960	0.00666
NM_001267550.2(TTN):c.21019A>T (p.Ile7007Phe)	rs114626713	0.00491
NM_001267550.2(TTN):c.21173G>A (p.Gly7058Asp)	rs72648964	0.00354
NM_001267550.2(TTN):c.21404-4A>G	rs72648965	0.00051
NM_001267550.2(TTN):c.21364G>A (p.Ala7122Thr)	rs201394117	0.00042
NM_001267550.2(TTN):c.21148C>T (p.Leu7050=)	rs202089818	0.00039
NM_001267550.2(TTN):c.20874G>A (p.Thr6958=)	rs765956215	0.00004
NM_001267550.2(TTN):c.21157A>C (p.Thr7053Pro)	rs727504741	0.00001

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