List of variants in gene TTR reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.201-32C>T	rs189979926	0.00417
NM_000371.4(TTR):c.336+19G>A	rs75517067	0.00309
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074	0.00040
NM_000371.4(TTR):c.69+30C>T	rs377167174	0.00011
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.336+18C>T	rs370628373	0.00005
NM_000371.4(TTR):c.200+20T>C	rs2073494875	0.00001
NM_000371.4(TTR):c.70-16T>C	rs759512847	0.00001
NM_000371.4(TTR):c.120C>T (p.Val40=)
NM_000371.4(TTR):c.201-27C>A	rs1315540051
NM_000371.4(TTR):c.9T>C (p.Ser3=)	rs1598843600

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