List of variants in gene TTN reported as uncertain significance for Dilated cardiomyopathy 1S

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.55745C>T (p.Pro18582Leu)	rs201194435	0.00011
NM_001267550.2(TTN):c.25570G>A (p.Gly8524Arg)	rs371512914	0.00010
NM_001267550.2(TTN):c.74305A>G (p.Asn24769Asp)	rs372787601	0.00005
NM_001267550.2(TTN):c.98759G>A (p.Arg32920Gln)	rs752015224	0.00004
NM_001267550.2(TTN):c.54140C>T (p.Ala18047Val)	rs373815064	0.00003
NM_001267550.2(TTN):c.106403T>A (p.Leu35468His)	rs952475900	0.00001
NM_001267550.2(TTN):c.11887G>A (p.Gly3963Arg)	rs1000514079	0.00001
NM_001267550.2(TTN):c.92595A>C (p.Leu30865Phe)	rs192086736	0.00001
NM_001267550.2(TTN):c.101774_101776dup (p.Glu33925dup)	rs1553497680
NM_001267550.2(TTN):c.41486G>C (p.Gly13829Ala)	rs1114167326
NM_001267550.2(TTN):c.521A>G (p.Tyr174Cys)	rs1114167334
NM_001267550.2(TTN):c.83062C>T (p.Arg27688Cys)	rs757441189
NM_001267550.2(TTN):c.86637T>A (p.Asn28879Lys)	rs1114167328

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