List of variants in gene TTR 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.384C>T (p.Ala128=)	rs143906738	0.00013
NM_000371.4(TTR):c.354C>T (p.Asn118=)	rs11541797	0.00009
NM_000371.4(TTR):c.70-7C>T	rs587780990	0.00005
NM_000371.4(TTR):c.405C>G (p.Ser135=)	rs760153126	0.00003
NM_000371.4(TTR):c.231G>A (p.Gly77=)	rs1555631396

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