List of variants in gene TTN reported as likely pathogenic by Genetics and Genomics Program, Sidra Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.40608del (p.Lys13536fs)	rs1284446305
NM_001267550.2(TTN):c.54327del (p.Lys18110fs)	rs2054381012
NM_001267550.2(TTN):c.73828_73835del (p.Val24611fs)	rs1708504899
NM_001267550.2(TTN):c.91097_91100del (p.Arg30366fs)	rs769422187

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