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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.336+19G>A	rs75517067	0.00309
NM_000371.4(TTR):c.416C>T (p.Thr139Met)	rs28933981	0.00177
NM_000371.4(TTR):c.360C>T (p.Ser120=)	rs150127220	0.00128
NM_000371.4(TTR):c.417G>A (p.Thr139=)	rs2276382	0.00104
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074	0.00040
NM_000371.4(TTR):c.371G>A (p.Arg124His)	rs121918095	0.00019
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.437A>G (p.Lys146Arg)	rs536294863	0.00005
NM_000371.4(TTR):c.70-9T>C	rs764059061	0.00003
NM_000371.4(TTR):c.24C>T (p.Leu8=)	rs991342939	0.00001
NM_000371.4(TTR):c.408T>C (p.Tyr136=)	rs1454790119	0.00001
NM_000371.4(TTR):c.70-16T>C	rs759512847	0.00001
NM_000371.4(TTR):c.337-14_337-11del	rs112263266
NM_000371.4(TTR):c.372C>G (p.Arg124=)	rs780119793

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