List of variants in gene combination LOC126806431, 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.17312C>G (p.Thr5771Ser)	rs16866477	0.00593
NM_001267550.2(TTN):c.17048A>G (p.Tyr5683Cys)	rs72648942	0.00471
NM_001267550.2(TTN):c.17183-9T>C	rs141687561	0.00133
NM_001267550.2(TTN):c.17115C>T (p.Gly5705=)	rs370036981	0.00061
NM_001267550.2(TTN):c.17543G>A (p.Gly5848Glu)	rs185962498	0.00028
NM_001267550.2(TTN):c.17183-7C>T	rs371785683	0.00009
NM_001267550.2(TTN):c.16904-8dup

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