List of variants in gene TTR reported as benign by Breakthrough Genomics, Breakthrough Genomics

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.337-18G>C	rs36204272	0.06198
NM_000371.4(TTR):c.76G>A (p.Gly26Ser)	rs1800458	0.05166
NM_000371.4(TTR):c.201-76T>A	rs59882235	0.04134
NM_000371.4(TTR):c.*21C>A	rs12226	0.02158
NM_000371.3(TTR):c.*191C>T	rs556327750	0.00023

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