List of variants in gene TTR reported as benign for not specified

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: 20

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000371.4(TTR):c.337-18G>C	rs36204272	0.06198
NM_000371.4(TTR):c.76G>A (p.Gly26Ser)	rs1800458	0.05166
NM_000371.4(TTR):c.336+19G>A	rs75517067	0.00289
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.3_11del	rs143948820	0.00076
NM_000371.4(TTR):c.328C>A (p.His110Asn)	rs121918074	0.00038
NM_000371.4(TTR):c.371G>A (p.Arg124His)	rs121918095	0.00032
NM_000371.4(TTR):c.384C>T (p.Ala128=)	rs143906738	0.00013
NM_000371.4(TTR):c.354C>T (p.Asn118=)	rs11541797	0.00009
NM_000371.4(TTR):c.70-7C>T	rs587780990	0.00005
NM_000371.4(TTR):c.70-9T>C	rs764059061	0.00003
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.337-475T>A
NM_000371.4(TTR):c.337-475T>G	rs75717327
NM_000371.4(TTR):c.337-496T>A	rs996830405
NM_000371.4(TTR):c.372C>G (p.Arg124=)	rs780119793

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.