List of variants in gene combination LOC126806428, TTN reported as likely pathogenic for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.21116-1G>A	rs771575556	0.00002
NM_001267550.2(TTN):c.21118C>T (p.Arg7040Ter)	rs576359448	0.00001
NM_001267550.2(TTN):c.21142C>T (p.Arg7048Ter)	rs770579313	0.00001
NM_001267550.2(TTN):c.21403+2T>G	rs2078872337	0.00001
NM_001267550.2(TTN):c.20837-1G>A	rs1553914337
NM_001267550.2(TTN):c.21004del (p.Ile7002fs)
NM_001267550.2(TTN):c.21006del (p.Ser7003fs)	rs2529622989
NM_001267550.2(TTN):c.21014T>G (p.Leu7005Ter)	rs2529622298
NM_001267550.2(TTN):c.21220del (p.Ser7074fs)	rs2078907250
NM_001267550.2(TTN):c.21313del (p.Ser7105fs)
NM_001267550.2(TTN):c.21404-1G>C	rs1433170500

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