IL1B c.656A>G ;(p.K219R)

Variant ID: 2-113588092-T-C

NM_000576.2(IL1B):c.656A>G;(p.K219R)

This variant was identified in 1 publication

View GRCh38 version.




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: IL1B: Lys219Arg
PubMed Link: 18620593
Variant Present in the following documents:
  • Main text
View BVdb publication page