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PPARG c.40G>C ;(p.G14R)
Variant ID: 3-12421250-G-C
NM_138711.3(
PPARG
):c.40G>C;(p.G14R)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetic Markers Associated with Power Athlete Status.
Journal Of Human Kinetics
Maciejewska-Skrendo, Agnieszka A; Cięszczyk, Paweł P; Chycki, Jakub J; Sawczuk, Marek M; Smółka, Wojciech W
Publication Date: 2019-08
Variant appearance in text: PPARG: Gly16Arg
PubMed Link:
31531130
Variant Present in the following documents:
hukin-68-017.pdf
View BVdb publication page
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: PPARG: Gly16Arg
PubMed Link:
18620593
Variant Present in the following documents:
Main text
View BVdb publication page
Human nutrition and food research: opportunities and challenges in the post-genomic era.
Philosophical Transactions Of The Royal Society Of London. Series B, Biological Sciences
Fairweather-Tait, Susan J SJ
Publication Date: 2003-10-29
Variant appearance in text: PPARgamma: Gly16Arg
PubMed Link:
14561328
Variant Present in the following documents:
Main text
View BVdb publication page