ClinVar Miner

List of variants in gene combination LOC126806428, TTN reported as likely benign for Early-onset myopathy with fatal cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.21019A>T (p.Ile7007Phe)	rs114626713	0.00491
NM_001267550.2(TTN):c.21173G>A (p.Gly7058Asp)	rs72648964	0.00335

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