PNPLA3 c.696+111C>A

Variant ID: 22-44329078-C-A

NM_025225.2(PNPLA3):c.696+111C>A

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study.

Gut
Buch, Stephan S; Innes, Hamish H; Lutz, Philipp Ludwig PL; Nischalke, Hans Dieter HD; Marquardt, Jens U JU; Fischer, Janett J; Weiss, Karl Heinz KH; Rosendahl, Jonas J; Marot, Astrid A; Krawczyk, Marcin M; Casper, Markus M; Lammert, Frank F; Eyer, Florian F; Vogel, Arndt A; Marhenke, Silke S; von Felden, Johann J; Sharma, Rohini R; Atkinson, Stephen Rahul SR; McQuillin, Andrew A; Nattermann, Jacob J; Schafmayer, Clemens C; Franke, Andre A; Strassburg, Christian C; Rietschel, Marcella M; Altmann, Heidi H; Sulk, Stefan S; Thangapandi, Veera Raghavan VR; Brosch, Mario M; Lackner, Carolin C; Stauber, Rudolf E RE; Canbay, Ali A; Link, Alexander A; Reiberger, Thomas T; Mandorfer, Mattias M; Semmler, Georg G; Scheiner, Bernhard B; Datz, Christian C; Romeo, Stefano S; Ginanni Corradini, Stefano S; Irving, William Lucien WL; Morling, Joanne R JR; Guha, Indra Neil IN; Barnes, Eleanor E; Ansari, M Azim MA; Quistrebert, Jocelyn J; Valenti, Luca L; Müller, Sascha A SA; Morgan, Marsha Yvonne MY; Dufour, Jean-François JF; Trebicka, Jonel J; Berg, Thomas T; Deltenre, Pierre P; Mueller, Sebastian S; Hampe, Jochen J; Stickel, Felix F
Publication Date: 2022-07-04

Variant appearance in text: rs2076211
PubMed Link: 35788059
Variant Present in the following documents:
  • gutjnl-2022-327196supp001.pdf
View BVdb publication page



Multi-Trait Genome-Wide Association Study of Atherosclerosis Detects Novel Pleiotropic Loci.

Frontiers In Genetics
Bellomo, Tiffany R TR; Bone, William P WP; Chen, Brian Y BY; Gawronski, Katerina A B KAB; Zhang, David D; Park, Joseph J; Levin, Michael M; Tsao, Noah N; Klarin, Derek D; Lynch, Julie J; Assimes, Themistocles L TL; Gaziano, J Michael JM; Wilson, Peter W PW; Cho, Kelly K; Vujkovic, Marijana M; O'Donnell, Christopher J CJ; Chang, Kyong-Mi KM; Tsao, Philip S PS; Rader, Daniel J DJ; Ritchie, Marylyn D MD; Damrauer, Scott M SM; Voight, Benjamin F BF
Publication Date: 2021

Variant appearance in text: rs2076211
PubMed Link: 35186008
Variant Present in the following documents:
  • Main text
  • fgene-12-787545.pdf
View BVdb publication page



Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD.

Hepatology Communications
Wegermann, Kara K; Garrett, Melanie E ME; Zheng, Jiayin J; Coviello, Andrea A; Moylan, Cynthia A CA; Abdelmalek, Manal F MF; Chow, Shein-Chung SC; Guy, Cynthia D CD; Diehl, Anna Mae AM; Ashley-Koch, Allison A; Suzuki, Ayako A
Publication Date: 2021-04

Variant appearance in text: rs2076211
PubMed Link: 33860118
Variant Present in the following documents:
  • Main text
View BVdb publication page



Liver enzymes, metabolomics and genome-wide association studies: from systems biology to the personalized medicine.

World Journal Of Gastroenterology
Sookoian, Silvia S; Pirola, Carlos J CJ
Publication Date: 2015-01-21

Variant appearance in text: rs2076211
PubMed Link: 25624707
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.

Plos One
Kawaguchi, Takahisa T; Sumida, Yoshio Y; Umemura, Atsushi A; Matsuo, Keitaro K; Takahashi, Meiko M; Takamura, Toshinari T; Yasui, Kohichiroh K; Saibara, Toshiji T; Hashimoto, Etsuko E; Kawanaka, Miwa M; Watanabe, Sumio S; Kawata, Sumio S; Imai, Yasuharu Y; Kokubo, Miki M; Shima, Toshihide T; Park, Hyohun H; Tanaka, Hideo H; Tajima, Kazuo K; Yamada, Ryo R; Matsuda, Fumihiko F; Okanoue, Takeshi T; ,
Publication Date: 2012

Variant appearance in text: rs2076211
PubMed Link: 22719876
Variant Present in the following documents:
  • Main text
  • pone.0038322.pdf
View BVdb publication page