List of variants in gene TTN reported as uncertain significance for long QT syndrome

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.59113C>T (p.Arg19705Cys)	rs72646839	0.00024
NM_001267550.2(TTN):c.12845T>A (p.Ile4282Asn)	rs747907234	0.00004
NM_001267550.2(TTN):c.42851G>A (p.Arg14284His)	rs368572799	0.00004
NM_001267550.2(TTN):c.86974T>C (p.Cys28992Arg)	rs769162510	0.00003
NM_001267550.2(TTN):c.58858A>G (p.Thr19620Ala)	rs1215190215	0.00001
NM_001267550.2(TTN):c.75923C>T (p.Pro25308Leu)	rs776006935	0.00001
NM_001267550.2(TTN):c.41038G>A (p.Ala13680Thr)	rs1576748259
NM_001267550.2(TTN):c.67271A>G (p.Tyr22424Cys)

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