Variants in gene TTR with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 2

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074	0.00038
NM_000371.4(TTR):c.88T>C (p.Cys30Arg)	rs121918083	0.00001

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