List of variants in gene combination LOC126806420, 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.100096G>A (p.Val33366Ile)	rs55675869	0.02132
NM_001267550.2(TTN):c.100094G>A (p.Arg33365Gln)	rs55742743	0.01280
NM_001267550.2(TTN):c.100059T>A (p.Ile33353=)	rs56026369	0.00099
NM_001267550.2(TTN):c.99901G>A (p.Glu33301Lys)	rs72648278	0.00041
NM_001267550.2(TTN):c.99866-10C>T	rs773128928	0.00034
NM_001267550.2(TTN):c.99991T>C (p.Cys33331Arg)	rs56061641	0.00022
NM_001267550.2(TTN):c.99969C>T (p.Ile33323=)	rs375403439	0.00016
NM_001267550.2(TTN):c.100315T>C (p.Trp33439Arg)	rs545443009	0.00006
NM_001267550.2(TTN):c.99900C>T (p.Ile33300=)	rs747130957	0.00001
NM_001267550.2(TTN):c.99810C>T (p.Val33270=)	rs564536939

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