Variants in gene TTR with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.336+19G>A	rs75517067	0.00309
NM_000371.4(TTR):c.417G>A (p.Thr139=)	rs2276382	0.00104
NM_000371.4(TTR):c.14G>A (p.Arg5His)	rs138657343	0.00017
NM_000371.4(TTR):c.384C>T (p.Ala128=)	rs143906738	0.00015
NM_000371.4(TTR):c.354C>T (p.Asn118=)	rs11541797	0.00009
NM_000371.4(TTR):c.355G>A (p.Asp119Asn)	rs76410435	0.00006
NM_000371.4(TTR):c.70-9T>C	rs764059061	0.00003
NM_000371.4(TTR):c.-3A>G	rs745422404	0.00002
NM_000371.4(TTR):c.439G>T (p.Glu147Ter)	rs730881162	0.00002
NM_000371.4(TTR):c.69G>A (p.Thr23=)	rs752579437	0.00001
NM_000371.4(TTR):c.70-16T>C	rs759512847	0.00001
NM_000371.4(TTR):c.*9TCC[1]	rs766223850
NM_000371.4(TTR):c.337-14_337-11del	rs112263266

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