LRP1B c.2887+8468A>C

Variant ID: 2-141731261-T-G

NM_018557.2(LRP1B):c.2887+8468A>C

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:

Genetic Variants behind Cardiovascular Diseases and Dementia.

Genes
Ho, Wei-Min WM; Wu, Yah-Yuan YY; Chen, Yi-Chun YC
Publication Date: 2020-12-18

Variant appearance in text: rs980286
PubMed Link: 33352859
Variant Present in the following documents:
  • Main text
  • genes-11-01514.pdf
View BVdb publication page