List of variants in gene combination LOC126806422, TTN reported as uncertain significance 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.70102A>G (p.Ile23368Val)	rs367914610	0.00005
NM_001267550.2(TTN):c.70424G>A (p.Arg23475His)	rs370257707	0.00004
NM_001267550.2(TTN):c.69637C>T (p.Arg23213Cys)	rs1335495074	0.00001
NM_001267550.2(TTN):c.69815T>G (p.Ile23272Ser)	rs758398301	0.00001
NM_001267550.2(TTN):c.70181C>T (p.Thr23394Met)	rs397517683	0.00001
NM_001267550.2(TTN):c.70231G>A (p.Gly23411Ser)	rs767075037	0.00001
NM_001267550.2(TTN):c.69738T>G (p.Asn23246Lys)	rs2154172948
NM_001267550.2(TTN):c.69976G>A (p.Glu23326Lys)
NM_001267550.2(TTN):c.70178_70180dup (p.Asn23393dup)	rs2154172646
NM_001267550.2(TTN):c.70327C>G (p.Arg23443Gly)	rs765987438

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