PPARG c.1180+3371G>A

Variant ID: 3-12462024-G-A

NM_138711.6(PPARG):c.1180+3371G>A

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Intake of Total and Subgroups of Fat Minimally Affect the Associations between Selected Single Nucleotide Polymorphisms in the PPARγ Pathway and Changes in Anthropometry among European Adults from Cohorts of the DiOGenes Study.

The Journal Of Nutrition
Larsen, Sofus C SC; Ängquist, Lars L; Østergaard, Jane N JN; Ahluwalia, Tarunveer S TS; Vimaleswaran, Karani S KS; Roswall, Nina N; Mortensen, Lotte M LM; Nielsen, Birgit M BM; Tjønneland, Anne A; Wareham, Nicholas J NJ; Palli, Domenico D; Masala, Giovanna G; Saris, Wim H M WH; van der A, Daphne L DL; Boer, Jolanda M A JM; Feskens, Edith J M EJ; Boeing, Heiner H; Jakobsen, Marianne U MU; Loos, Ruth J F RJ; Sørensen, Thorkild I A TI; Overvad, Kim K
Publication Date: 2016-03

Variant appearance in text: rs709157
PubMed Link: 26865646
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common genetic variants in peroxisome proliferator-activated receptor-γ (PPARG) and type 2 diabetes risk among Women's Health Initiative postmenopausal women.

The Journal Of Clinical Endocrinology And Metabolism
Chan, Kei Hang K KH; Niu, Tianhua T; Ma, Yunsheng Y; You, Nai-chieh Y NC; Song, Yiqing Y; Sobel, Eric M EM; Hsu, Yi-Hsiang YH; Balasubramanian, Raji R; Qiao, Yongxia Y; Tinker, Lesley L; Liu, Simin S
Publication Date: 2013-03

Variant appearance in text: rs709157
PubMed Link: 23386649
Variant Present in the following documents:
  • Main text
View BVdb publication page



HTR1B, ADIPOR1, PPARGC1A, and CYP19A1 and obesity in a cohort of Caucasians and African Americans: an evaluation of gene-environment interactions and candidate genes.

American Journal Of Epidemiology
Edwards, Todd L TL; Velez Edwards, Digna R DR; Villegas, Raquel R; Cohen, Sarah S SS; Buchowski, Maciej S MS; Fowke, Jay H JH; Schlundt, David D; Long, Jirong J; Long, Ji Rong JR; Cai, Qiuyin Q; Zheng, Wei W; Shu, Xiao-Ou XO; Hargreaves, Margaret K MK; Smith, Jeffrey J; Jeffrey, Smith S; Williams, Scott M SM; Signorello, Lisa B LB; Blot, William J WJ; Matthews, Charles E CE
Publication Date: 2012-01-01

Variant appearance in text: rs709157
PubMed Link: 22106445
Variant Present in the following documents:
  • Main text
View BVdb publication page



Candidate gene polymorphisms for ischemic stroke.

Stroke
Matarin, Mar M; Brown, W Mark WM; Dena, Hernandez H; Britton, Angela A; De Vrieze, Fabienne Wavrant FW; Brott, Thomas G TG; Brown, Robert D RD; Worrall, Bradford B BB; Case, L Douglas LD; Chanock, Stephen J SJ; Metter, E Jeffrey EJ; Ferruci, Luigi L; Gamble, Dale D; Hardy, John A JA; Rich, Stephen S SS; Singleton, Andrew A; Meschia, James F JF
Publication Date: 2009-11

Variant appearance in text: rs709157
PubMed Link: 19729601
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women.

Osteoporosis International : A Journal Established As Result Of Cooperation Between The European Foundation For Osteoporosis And The National Osteoporosis Foundation Of The Usa
Li, G H Y GH; Kung, A W C AW; Huang, Q-Y QY
Publication Date: 2010-06

Variant appearance in text: rs709157
PubMed Link: 19727905
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia.

Arteriosclerosis, Thrombosis, And Vascular Biology
Mar-Heyming, Rebecca R; Miyazaki, Makoto M; Weissglas-Volkov, Daphna D; Kolaitis, Nicholas A NA; Sadaat, Narimaan N; Plaisier, Christopher C; Pajukanta, Päivi P; Cantor, Rita M RM; de Bruin, Tjerk W A TW; Ntambi, James M JM; Lusis, Aldons J AJ
Publication Date: 2008-06

Variant appearance in text: rs709157
PubMed Link: 18340007
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.

Bmc Medical Genetics
Fox, Caroline S CS; Heard-Costa, Nancy N; Cupples, L Adrienne LA; Dupuis, Josée J; Vasan, Ramachandran S RS; Atwood, Larry D LD
Publication Date: 2007-09-19

Variant appearance in text: rs709157
PubMed Link: 17903300
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association with diabetes-related traits in the Framingham Heart Study.

Bmc Medical Genetics
Meigs, James B JB; Manning, Alisa K AK; Fox, Caroline S CS; Florez, Jose C JC; Liu, Chunyu C; Cupples, L Adrienne LA; Dupuis, Josée J
Publication Date: 2007-09-19

Variant appearance in text: rs709157
PubMed Link: 17903298
Variant Present in the following documents:
  • Main text
View BVdb publication page



A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.

Bmc Medical Genetics
Hwang, Shih-Jen SJ; Yang, Qiong Q; Meigs, James B JB; Pearce, Elizabeth N EN; Fox, Caroline S CS
Publication Date: 2007-09-19

Variant appearance in text: rs709157
PubMed Link: 17903292
Variant Present in the following documents:
  • Main text
  • 1471-2350-8-S1-S10.pdf
View BVdb publication page