List of variants in gene combination LOC126806422, TTN studied for Primary dilated cardiomyopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.69630C>A (p.Tyr23210Ter)	rs777602537
NM_001267550.2(TTN):c.69639dup (p.Val23214fs)	rs869025557
NM_001267550.2(TTN):c.69783G>A (p.Trp23261Ter)	rs730880241
NM_001267550.2(TTN):c.69843del (p.Lys23281_Val23282insTer)	rs869312075
NM_001267550.2(TTN):c.69877G>T (p.Gly23293Ter)	rs869312114
NM_001267550.2(TTN):c.70045G>T (p.Glu23349Ter)
NM_001267550.2(TTN):c.70051C>T (p.Arg23351Ter)	rs1060500575
NM_001267550.2(TTN):c.70274G>C (p.Ser23425Thr)	rs980974415
NM_001267550.2(TTN):c.70275del (p.Ser23425fs)	rs727504655
NM_001267550.2(TTN):c.70476C>A (p.Cys23492Ter)

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