List of variants in gene TTN reported as benign for cardiac rhythm disease

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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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.104377A>C (p.Met34793Leu)	rs72629787	0.00909
NM_001267550.2(TTN):c.101766G>C (p.Gln33922His)	rs55886356	0.00774
NM_001267550.2(TTN):c.57464G>A (p.Arg19155Lys)	rs72646833	0.00702
NM_001267550.2(TTN):c.32624C>T (p.Pro10875Leu)	rs72650031	0.00544
NM_001267550.2(TTN):c.47723G>A (p.Arg15908His)	rs72677237	0.00519
NM_001267550.2(TTN):c.9359G>A (p.Arg3120Gln)	rs72647894	0.00404
NM_001267550.2(TTN):c.25978G>A (p.Val8660Ile)	rs141856116	0.00372
NM_001267550.2(TTN):c.58636G>C (p.Glu19546Gln)	rs201840554	0.00323
NM_001267550.2(TTN):c.47315G>A (p.Arg15772Gln)	rs72677233	0.00287
NM_001267550.2(TTN):c.5231C>T (p.Pro1744Leu)	rs75686037	0.00202
NM_001267550.2(TTN):c.8902+14T>A	rs13388274	0.00134
NM_001267550.2(TTN):c.87877C>T (p.Arg29293Cys)	rs191482653	0.00057

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