LRP1 c.755C>G ;(p.A252G)

Variant ID: 12-57539187-C-G

NM_002332.2(LRP1):c.755C>G;(p.A252G)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome.

Bmc Medical Genetics
Morgan, Thomas M TM; Xiao, Lan L; Lyons, Patrick P; Kassebaum, Bethany B; Krumholz, Harlan M HM; Spertus, John A JA
Publication Date: 2008-07-12

Variant appearance in text: LRP1: A252G
PubMed Link: 18620593
Variant Present in the following documents:
  • Main text
  • 1471-2350-9-66.pdf
View BVdb publication page