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