List of variants in gene combination LOC126806426, TTN reported as benign 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.48996G>A (p.Glu16332=)	rs72677244	0.03561
NM_001267550.2(TTN):c.48727C>T (p.Pro16243Ser)	rs72677242	0.00641
NM_001267550.2(TTN):c.49200G>A (p.Lys16400=)	rs539513077	0.00028

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