List of variants in gene VLDLR reported as likely 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: 26

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003383.5(VLDLR):c.2416+8G>T	rs6145	0.24562
NM_003383.5(VLDLR):c.1187-3C>T	rs11789583	0.15129
NM_003383.5(VLDLR):c.2067A>G (p.Gln689=)	rs6148	0.13882
NM_003383.5(VLDLR):c.175G>A (p.Val59Ile)	rs6149	0.05632
NM_003383.5(VLDLR):c.944-5T>C	rs35782329	0.03136
NM_003383.5(VLDLR):c.464G>C (p.Ser155Thr)	rs34080096	0.00311
NM_003383.5(VLDLR):c.2291C>T (p.Thr764Met)	rs56737058	0.00223
NM_003383.5(VLDLR):c.1162C>T (p.Leu388=)	rs114172780	0.00146
NM_003383.5(VLDLR):c.902G>A (p.Arg301Gln)	rs139671268	0.00141
NM_003383.5(VLDLR):c.242A>G (p.Asn81Ser)	rs140526335	0.00115
NM_003383.5(VLDLR):c.943+19T>C	rs144551353	0.00078
NM_003383.5(VLDLR):c.468C>T (p.Pro156=)	rs2242105	0.00058
NM_003383.5(VLDLR):c.1313G>A (p.Gly438Asp)	rs200605669	0.00050
NM_003383.5(VLDLR):c.1704-17C>T	rs149818793	0.00031
NM_003383.5(VLDLR):c.2104+5C>T	rs201953557	0.00022
NM_003383.5(VLDLR):c.738C>T (p.Cys246=)	rs116687040	0.00020
NM_003383.5(VLDLR):c.1650G>T (p.Leu550=)	rs753725484	0.00006
NM_003383.5(VLDLR):c.2085T>C (p.His695=)	rs748367754	0.00003
NM_003383.5(VLDLR):c.672G>A (p.Glu224=)	rs762512932	0.00001
NM_003383.5(VLDLR):c.-19_-18insGGCACC	rs1554617689
NM_003383.5(VLDLR):c.-42GGC[6]	rs71329437
NM_003383.5(VLDLR):c.-42GGC[9]	rs71329437
NM_003383.5(VLDLR):c.1788A>G (p.Thr596=)	rs1057522727
NM_003383.5(VLDLR):c.2223T>C (p.Asn741=)	rs374758758
NM_003383.5(VLDLR):c.449-10C>G	rs1554620947
NM_003383.5(VLDLR):c.471C>T (p.Asp157=)	rs138649440

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.