List of variants in gene TTR reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.280G>C (p.Asp94His)	rs730881164	0.00007
NM_000371.4(TTR):c.385G>A (p.Ala129Thr)	rs267607159	0.00005
NM_000371.4(TTR):c.370C>T (p.Arg124Cys)	rs745834030	0.00003
NM_000371.4(TTR):c.-1G>C	rs769343676	0.00002
NM_000371.4(TTR):c.201-16C>T	rs941725460	0.00001
NM_000371.4(TTR):c.301G>A (p.Ala101Thr)	rs730881165	0.00001
NM_000371.4(TTR):c.69G>A (p.Thr23=)	rs752579437	0.00001
NM_000371.4(TTR):c.*9TCC[1]	rs766223850
NM_000371.4(TTR):c.186G>T (p.Glu62Asp)	rs1340627860
NM_000371.4(TTR):c.302C>T (p.Ala101Val)	rs1555631417
NM_000371.4(TTR):c.418G>T (p.Ala140Ser)	rs876658108
NM_000371.4(TTR):c.69+6T>C
NM_000371.4(TTR):c.88T>G (p.Cys30Gly)

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