List of variants in gene combination LOC101927055, TTN reported as uncertain significance for Dilated cardiomyopathy 1G

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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.4199G>C (p.Ser1400Thr)	rs138506461	0.00219
NM_001267550.2(TTN):c.4396T>C (p.Phe1466Leu)	rs151310601	0.00089
NM_001267550.2(TTN):c.4668G>A (p.Pro1556=)	rs145709534	0.00011
NM_001267550.2(TTN):c.4087A>G (p.Thr1363Ala)	rs768249663	0.00004
NM_001267550.2(TTN):c.4639G>A (p.Val1547Met)	rs750678272	0.00002
NM_001267550.2(TTN):c.4031A>G (p.Asp1344Gly)	rs1203373476	0.00001
NM_001267550.2(TTN):c.4076A>G (p.Glu1359Gly)	rs370978752	0.00001
NM_001267550.2(TTN):c.4292G>A (p.Arg1431Gln)	rs373690688	0.00001
NM_001267550.2(TTN):c.4874C>G (p.Ser1625Cys)	rs185789611	0.00001
NM_001267550.2(TTN):c.4319G>T (p.Gly1440Val)	rs150579194
NM_001267550.2(TTN):c.4322G>A (p.Arg1441His)	rs72647876
NM_001267550.2(TTN):c.4506C>T (p.Thr1502=)	rs185660585
NM_001267550.2(TTN):c.4724_4728del (p.Met1575fs)	rs756433029

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