ClinVar Miner

List of variants in gene LRP5 reported by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 14
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002335.4(LRP5):c.1647T>C (p.Phe549=) rs545382 0.83202
NM_002335.4(LRP5):c.3357G>A (p.Val1119=) rs556442 0.55735
NM_002335.4(LRP5):c.884-4T>C rs314776 0.48379
NM_002335.4(LRP5):c.1412+8G>A rs4988319 0.15090
NM_002335.4(LRP5):c.2220C>T (p.Asn740=) rs2306862 0.11683
NM_002335.4(LRP5):c.3989C>T (p.Ala1330Val) rs3736228 0.10701
NM_002335.4(LRP5):c.2318+6T>C rs4988322 0.06393
NM_002335.4(LRP5):c.1932G>A (p.Glu644=) rs2277268 0.06342
NM_002335.4(LRP5):c.3297C>T (p.Asp1099=) rs17149104 0.02225
NM_002335.4(LRP5):c.4431C>T (p.His1477=) rs11574426 0.00238
NM_002335.4(LRP5):c.4089C>T (p.Asp1363=) rs3736229 0.00195
NM_002335.4(LRP5):c.1413-7T>A rs141889567 0.00077
NM_002335.4(LRP5):c.291C>T (p.Ala97=) rs146667935 0.00061
NM_002335.4(LRP5):c.1828G>A (p.Gly610Arg) rs80358313

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.