List of variants in gene combination LOC126806423, TTN reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67495C>T (p.Arg22499Ter)	rs574660186	0.00004
NM_001267550.2(TTN):c.68286_68289dup (p.Trp22764fs)	rs2154174801
NM_001267550.2(TTN):c.68308del (p.Thr22770fs)	rs1064796112

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