Variant ID: 16-57012379-T-G

NM_000078.2(CETP):c.1146+212T>G

This variant was identified in 19 publications




Publications:


Effects of Obesity and Family History of Diabetes on the Association of CETP rs6499861 with HDL-C Level in Korean Populations.

Journal Of Lipid And Atherosclerosis
JW Sull, S Kim, SH Jee
Publication Date: 2019-09

Variant appearance in text: rs12708980
PubMed Link: 32821715
Variant Present in the following documents:
  • Main text
View BVdb publication page



New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population.

Scientific Reports
HS Lee, Y Kim, T Park
Publication Date: 2018-04-09

Variant appearance in text: rs12708980
PubMed Link: 29632305
Variant Present in the following documents:
  • 41598_2018_23074_MOESM1_ESM.docx
  • aaaaaMain text
View BVdb publication page



From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results.

Plos One
E Cirillo, M Kutmon, M Gonzalez Hernandez, T Hooimeijer, ME Adriaens, LMT Eijssen, LD Parnell, SL Coort, CT Evelo
Publication Date: 2018

Variant appearance in text: rs12708980
PubMed Link: 29617380
Variant Present in the following documents:
  • Complete_dissertation.pdf
View BVdb publication page



Identifying potentially common genes between dyslipidemia and osteoporosis using novel analytical approaches.

Molecular Genetics And Genomics : Mgg
X Lin, C Peng, J Greenbaum, ZF Li, KH Wu, ZX Ao, T Zhang, J Shen, HW Deng
Publication Date: 2018-06

Variant appearance in text: rs12708980
PubMed Link: 29327327
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

Plos Genetics
JP Davis, JR Huyghe, AE Locke, AU Jackson, X Sim, HM Stringham, TM Teslovich, RP Welch, C Fuchsberger, N Narisu, PS Chines, AJ Kangas, P Soininen, M Ala-Korpela, J Kuusisto, FS Collins, M Laakso, M Boehnke, KL Mohlke
Publication Date: 2017-10

Variant appearance in text: rs12708980
PubMed Link: 29084231
Variant Present in the following documents:
  • pgen.1007079.s010.xlsx
  • pgen.1007079.s011.xlsx
View BVdb publication page



A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration.

Scientific Reports
K Kawashima-Kumagai, K Yamashiro, M Yoshikawa, M Miyake, GCC Ming, Q Fan, JY Koh, M Saito, M Sugahara-Kuroda, M Oishi, Y Akagi-Kurashige, I Nakata, H Nakanishi, N Gotoh, A Oishi, H Tamura, S Ooto, A Tsujikawa, Y Kurimoto, T Sekiryu, F Matsuda, CC Khor, CY Cheng, TY Wong, N Yoshimura
Publication Date: 2017-08-03

Variant appearance in text: rs12708980
PubMed Link: 28775256
Variant Present in the following documents:
  • 41598_2017_7526_MOESM1_ESM.xls
View BVdb publication page



Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study.

Journal Of Cellular And Molecular Medicine
Y Zhu, D Zhang, D Zhou, Z Li, Z Li, L Fang, M Yang, Z Shan, H Li, J Chen, X Zhou, W Ye, S Yu, H Li, L Cai, C Liu, J Zhang, L Wang, Y Lai, L Ruan, Z Sun, S Zhang, H Wang, Y Liu, Y Xu, J Ling, C Xu, Y Zhang, D Lv, Z Yuan, J Zhang, Y Zhang, Y Shi, M Lai
Publication Date: 2017-06

Variant appearance in text: rs12708980
PubMed Link: 28371326
Variant Present in the following documents:
  • JCMM-21-1106-s002.xlsx
View BVdb publication page



c.*84G>A Mutation in CETP Is Associated with Coronary Artery Disease in South Indians.

Plos One
M Ganesan, S Nizamuddin, SK Katkam, K Kumaraswami, UK Hosad, LL Lobo, VK Kutala, K Thangaraj
Publication Date: 2016

Variant appearance in text: rs12708980
PubMed Link: 27768712
Variant Present in the following documents:
  • Main text
View BVdb publication page



Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.

Scientific Reports
JE Below, EJ Parra, ER Gamazon, J Torres, S Krithika, S Candille, Y Lu, A Manichakul, J Peralta-Romero, Q Duan, Y Li, AP Morris, O Gottesman, E Bottinger, XQ Wang, KD Taylor, YD Ida Chen, JI Rotter, SS Rich, RJ Loos, H Tang, NJ Cox, M Cruz, CL Hanis, A Valladares-Salgado
Publication Date: 2016-01-19

Variant appearance in text: rs12708980
PubMed Link: 26780889
Variant Present in the following documents:
  • srep19429-s3.xls
View BVdb publication page



Resequencing of the CETP gene in American whites and African blacks: Association of rare and common variants with HDL-cholesterol levels.

Metabolism: Clinical And Experimental
D Pirim, X Wang, V Niemsiri, ZH Radwan, CH Bunker, JE Hokanson, RF Hamman, MM Barmada, FY Demirci, MI Kamboh
Publication Date: 2016-01

Variant appearance in text: rs12708980
PubMed Link: 26683795
Variant Present in the following documents:
  • Main text
View BVdb publication page



Evaluation of transethnic fine mapping with population-specific and cosmopolitan imputation reference panels in diverse Asian populations.

European Journal Of Human Genetics : Ejhg
X Wang, CY Cheng, J Liao, X Sim, J Liu, KS Chia, ES Tai, P Little, CC Khor, T Aung, TY Wong, YY Teo
Publication Date: 2016-04

Variant appearance in text: rs12708980
PubMed Link: 26130488
Variant Present in the following documents:
  • ejhg2015150x4.xls
View BVdb publication page



On the analysis of a repeated measure design in genome-wide association analysis.

International Journal Of Environmental Research And Public Health
Y Lee, S Park, S Moon, J Lee, RC Elston, W Lee, S Won
Publication Date: 2014-11-28

Variant appearance in text: rs12708980
PubMed Link: 25464127
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cis and trans effects of human genomic variants on gene expression.

Plos Genetics
J Bryois, A Buil, DM Evans, JP Kemp, SB Montgomery, DF Conrad, KM Ho, S Ring, M Hurles, P Deloukas, G Davey Smith, ET Dermitzakis
Publication Date: 2014-07

Variant appearance in text: rs12708980
PubMed Link: 25010687
Variant Present in the following documents:
  • pgen.1004461.s012.xlsx
View BVdb publication page



Genetic risk score and adiposity interact to influence triglyceride levels in a cohort of Filipino women.

Nutrition & Diabetes
N Zubair, EJ Mayer-Davis, MA Mendez, KL Mohlke, KE North, LS Adair
Publication Date: 2014-06-16

Variant appearance in text: rs12708980
PubMed Link: 24932782
Variant Present in the following documents:
  • Main text
View BVdb publication page



Properties of local interactions and their potential value in complementing genome-wide association studies.

Plos One
W Wei, A Gyenesei, CA Semple, CS Haley
Publication Date: 2013

Variant appearance in text: rs12708980
PubMed Link: 23940718
Variant Present in the following documents:
  • Main text
View BVdb publication page



Single nucleotide polymorphisms in CETP, SLC46A1, SLC19A1, CD36, BCMO1, APOA5, and ABCA1 are significant predictors of plasma HDL in healthy adults.

Lipids In Health And Disease
AJ Clifford, G Rincon, JE Owens, JF Medrano, AJ Moshfegh, DJ Baer, JA Novotny
Publication Date: 2013-05-08

Variant appearance in text: rs12708980
PubMed Link: 23656756
Variant Present in the following documents:
  • Main text
View BVdb publication page



Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population.

Genomics & Informatics
MJ Go, JY Hwang, DJ Kim, HJ Lee, HB Jang, KH Park, J Song, JY Lee
Publication Date: 2012-06

Variant appearance in text: rs12708980
PubMed Link: 23105936
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cholesteryl Ester Transfer Protein (CETP) polymorphisms affect mRNA splicing, HDL levels, and sex-dependent cardiovascular risk.

Plos One
AC Papp, JK Pinsonneault, D Wang, LC Newman, Y Gong, JA Johnson, CJ Pepine, M Kumari, AD Hingorani, PJ Talmud, S Shah, SE Humphries, W Sadee
Publication Date: 2012

Variant appearance in text: rs12708980
PubMed Link: 22403620
Variant Present in the following documents:
  • pone.0031930.s010.docx
View BVdb publication page



A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.

Science (New York, N.Y.)
LJ Scott, KL Mohlke, LL Bonnycastle, CJ Willer, Y Li, WL Duren, MR Erdos, HM Stringham, PS Chines, AU Jackson, L Prokunina-Olsson, CJ Ding, AJ Swift, N Narisu, T Hu, R Pruim, R Xiao, XY Li, KN Conneely, NL Riebow, AG Sprau, M Tong, PP White, KN Hetrick, MW Barnhart, CW Bark, JL Goldstein, L Watkins, F Xiang, J Saramies, TA Buchanan, RM Watanabe, TT Valle, L Kinnunen, GR Abecasis, EW Pugh, KF Doheny, RN Bergman, J Tuomilehto, FS Collins, M Boehnke
Publication Date: 2007-06-01

Variant appearance in text: rs12708980
PubMed Link: 17463248
Variant Present in the following documents:
  • NIHMS322992-supplement-Scott2007_supp.pdf
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000200676.3 c.1146+212T>G - intron_variant - 11/15
ENST00000379780.2 c.966+212T>G - intron_variant - 10/14
ENST00000566128.1 c.951+212T>G - intron_variant - 11/15
NM_000078.3 c.1146+212T>G - intron_variant - 11/15
NM_001286085.2 c.966+212T>G - intron_variant - 10/14