APOB c.867A>T ;(p.E289D)

Variant ID: 2-21257725-T-A

NM_000384.2(APOB):c.867A>T;(p.E289D)

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:

Clinical Utility of a Coronary Heart Disease Risk Prediction Gene Score in UK Healthy Middle Aged Men and in the Pakistani Population.

Plos One
Beaney, Katherine E KE; Cooper, Jackie A JA; Ullah Shahid, Saleem S; Ahmed, Waqas W; Qamar, Raheel R; Drenos, Fotios F; Crockard, Martin A MA; Humphries, Steve E SE
Publication Date: 2015

Variant appearance in text: APOB: E289D
PubMed Link: 26133560
Variant Present in the following documents:
  • Main text
  • pone.0130754.pdf
View BVdb publication page