List of variants in gene combination LOC126806430, TTN reported as likely benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18561G>A (p.Ala6187=)	rs377556808	0.00004
NM_001267550.2(TTN):c.18618G>A (p.Lys6206=)	rs1348113407	0.00001
NM_001267550.2(TTN):c.18927C>G (p.Ala6309=)

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