List of variants in gene combination LOC126806426, TTN reported as likely benign for Cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.48838G>A (p.Ala16280Thr)	rs372911542	0.00006
NM_001267550.2(TTN):c.49041C>T (p.Asn16347=)	rs369981635	0.00002
NM_001267550.2(TTN):c.48690G>A (p.Lys16230=)	rs2470697642	0.00001
NM_001267550.2(TTN):c.49219G>A (p.Asp16407Asn)	rs771017148

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