List of variants in gene combination LOC126806420, TTN reported as benign for Early-onset myopathy with fatal cardiomyopathy

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.100096G>A (p.Val33366Ile)	rs55675869	0.02155
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.99866-10C>T	rs773128928	0.00029
NM_001267550.2(TTN):c.99969C>T (p.Ile33323=)	rs375403439	0.00016
NM_001267550.2(TTN):c.99810C>T (p.Val33270=)	rs564536939

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