List of variants in gene combination LOC126806424, 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.59319G>A (p.Glu19773=)	rs367622770	0.00039
NM_001267550.2(TTN):c.59456C>T (p.Thr19819Ile)	rs758287054	0.00005
NM_001267550.2(TTN):c.60138T>C (p.Tyr20046=)	rs1215527173	0.00004
NM_001267550.2(TTN):c.59859G>A (p.Ala19953=)	rs759120495	0.00003
NM_001267550.2(TTN):c.59534G>A (p.Arg19845His)	rs201457934	0.00002
NM_001267550.2(TTN):c.59484A>G (p.Pro19828=)	rs2469534567	0.00001
NM_001267550.2(TTN):c.59533C>T (p.Arg19845Cys)	rs1232069163	0.00001
NM_001267550.2(TTN):c.60027C>T (p.Ile20009=)	rs368279024	0.00001
NM_001267550.2(TTN):c.59707G>A (p.Asp19903Asn)	rs374163882

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