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PPARG c.1181-6808C>G
Variant ID: 3-12468589-C-G
NM_138711.6(
PPARG
):c.1181-6808C>G
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
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UCSC Genome Browser
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dbSNP
Publications:
Metabolic heritability at birth: implications for chronic disease research.
Human Genetics
Ryckman, Kelli K KK; Smith, Caitlin J CJ; Jelliffe-Pawlowski, Laura L LL; Momany, Allison M AM; Berberich, Stanton L SL; Murray, Jeffrey C JC
Publication Date: 2014-08
Variant appearance in text: rs13099828
PubMed Link:
24850141
Variant Present in the following documents:
Main text
View BVdb publication page
An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.
Plos One
Landa, Iñigo I; Boullosa, Cesar C; Inglada-Pérez, Lucía L; Sastre-Perona, Ana A; Pastor, Susana S; Velázquez, Antonia A; Mancikova, Veronika V; Ruiz-Llorente, Sergio S; Schiavi, Francesca F; Marcos, Ricard R; Malats, Nuria N; Opocher, Giuseppe G; Diaz-Uriarte, Ramon R; Santisteban, Pilar P; Valencia, Alfonso A; Robledo, Mercedes M
Publication Date: 2013
Variant appearance in text: rs13099828
PubMed Link:
24086368
Variant Present in the following documents:
Main text
pone.0074765.pdf
View BVdb publication page