List of variants in gene TTN reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.95245G>A (p.Glu31749Lys)	rs139542862	0.00013
NM_001267550.2(TTN):c.73391G>A (p.Arg24464Gln)	rs750056949	0.00006
NM_001267550.2(TTN):c.54178G>A (p.Val18060Ile)	rs190574498	0.00005
NM_001267550.2(TTN):c.66568G>C (p.Gly22190Arg)	rs757537780	0.00004
NM_001267550.2(TTN):c.85646C>T (p.Thr28549Ile)	rs774609232	0.00001
NM_001267550.2(TTN):c.89590A>G (p.Lys29864Glu)	rs770839822	0.00001
NM_001267550.2(TTN):c.33501AGA[6] (p.Glu11172dup)	rs368327166
NM_001267550.2(TTN):c.51260G>A (p.Arg17087Lys)	rs1576402466
NM_001267550.2(TTN):c.57399A>C (p.Leu19133Phe)	rs1576219060
NM_001267550.2(TTN):c.61447_61449del (p.Arg20483del)	rs775343508
NM_001267550.2(TTN):c.7954T>C (p.Trp2652Arg)	rs1574584723

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