LRP1B c.2887+9830G>T

Variant ID: 2-141729899-C-A

NM_018557.2(LRP1B):c.2887+9830G>T

This variant was identified in 1 publication

View GRCh38 version.




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: rs10201482
PubMed Link: 33352859
Variant Present in the following documents:
  • Main text
  • genes-11-01514.pdf
View BVdb publication page