MTHFR c.-14+1359A>G

Variant ID: 1-11864586-T-C

NM_005957.5(MTHFR):c.-14+1359A>G

This variant was identified in 13 publications

View GRCh38 version.




Publications:


The causal association between maternal smoking around birth on childhood asthma: A Mendelian randomization study.

Frontiers In Public Health
Ding, Zijun Z; Pang, Lei L; Chai, Hongqiang H; Li, Fei F; Wu, Ming M
Publication Date: 2022

Variant appearance in text: rs3753584
PubMed Link: 36408054
Variant Present in the following documents:
  • Main text
  • fpubh-10-1059195.pdf
View BVdb publication page



Association between NPPA promoter methylation and hypertension: results from Gusu cohort and replication in an independent sample.

Clinical Epigenetics
Li, Jing J; Zhu, Jinhua J; Ren, Liyun L; Ma, Shengqi S; Shen, Bin B; Yu, Jia J; Zhang, Rongyan R; Zhang, Mingzhi M; He, Yan Y; Peng, Hao H
Publication Date: 2020-09-03

Variant appearance in text: rs3753584
PubMed Link: 32883357
Variant Present in the following documents:
  • Main text
  • 13148_2020_Article_927.pdf
View BVdb publication page



A multiple coefficient of determination-based method for parsing SNPs that correlate with mRNA expression.

Scientific Reports
Song, Fan F; Tao, Yu Y; Sun, Yue Y; Saffen, David D
Publication Date: 2019-12-27

Variant appearance in text: rs3753584
PubMed Link: 31882953
Variant Present in the following documents:
  • 41598_2019_56494_MOESM1_ESM.pdf
View BVdb publication page



Association between methylenetetrahydrofolate reductase tagging polymorphisms and susceptibility of hepatocellular carcinoma: a case-control study.

Bioscience Reports
Zhang, Sheng S; Lin, Jing J; Jiang, Jiakai J; Chen, Yu Y; Tang, Weifeng W; Liu, Longgen L
Publication Date: 2019-11-29

Variant appearance in text: rs3753584
PubMed Link: 31694048
Variant Present in the following documents:
  • Main text
View BVdb publication page



The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population.

The American Journal Of Clinical Nutrition
Shane, Barry B; Pangilinan, Faith F; Mills, James L JL; Fan, Ruzong R; Gong, Tingting T; Cropp, Cheryl D CD; Kim, Yoonhee Y; Ueland, Per M PM; Bailey-Wilson, Joan E JE; Wilson, Alexander F AF; Brody, Lawrence C LC; Molloy, Anne M AM
Publication Date: 2018-12-01

Variant appearance in text: rs3753584
PubMed Link: 30339177
Variant Present in the following documents:
  • Main text
View BVdb publication page



Methylenetetrahydrofolate reductase tagging polymorphisms are associated with risk of esophagogastric junction adenocarcinoma: a case-control study involving 2,740 Chinese Han subjects.

Oncotarget
Ding, Guowen G; Wang, Yafeng Y; Chen, Yu Y; Yin, Jun J; Liu, Chao C; Fan, Yu Y; Qiu, Hao H; Tang, Weifeng W; Chen, Shuchen S
Publication Date: 2017-12-19

Variant appearance in text: rs3753584
PubMed Link: 29340069
Variant Present in the following documents:
  • Main text
  • oncotarget-08-111482.pdf
View BVdb publication page



Methylenetetrahydrofolate reductase tagging polymorphisms are associated with risk of non-small cell lung cancer in eastern Chinese Han population.

Oncotarget
Ding, Hao H; Wang, Yafeng Y; Chen, Yuanmei Y; Liu, Chao C; Qiu, Hao H; Kang, Mingqiang M; Tang, Weifeng W
Publication Date: 2017-12-15

Variant appearance in text: rs3753584
PubMed Link: 29299150
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population.

Circulation. Cardiovascular Genetics
Salo, Perttu P PP; Havulinna, Aki S AS; Tukiainen, Taru T; Raitakari, Olli O; Lehtimäki, Terho T; Kähönen, Mika M; Kettunen, Johannes J; Männikkö, Minna M; Eriksson, Johan G JG; Jula, Antti A; Blankenberg, Stefan S; Zeller, Tanja T; Salomaa, Veikko V; Kristiansson, Kati K; Perola, Markus M
Publication Date: 2017-12

Variant appearance in text: rs3753584
PubMed Link: 29237677
Variant Present in the following documents:
  • Main text
  • hcg-10-e001713-s001.pdf
  • hcg-10-e001713.pdf
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Investigation of methylenetetrahydrofolate reductase tagging polymorphisms with colorectal cancer in Chinese Han population.

Oncotarget
Zhang, Sheng S; Chen, Shuchen S; Chen, Yu Y; Kang, Mingqiang M; Liu, Chao C; Qiu, Hao H; Wang, Yafeng Y; Tang, Weifeng W
Publication Date: 2017-09-08

Variant appearance in text: rs3753584
PubMed Link: 28969008
Variant Present in the following documents:
  • Main text
  • oncotarget-08-63518.pdf
View BVdb publication page



Genetic variations in MTHFR and gastric cardia adenocarcinoma susceptibility in the Chinese Han population.

International Journal Of Clinical And Experimental Medicine
Wang, Yafeng Y; Chen, Shuchen S; Kang, Mingqiang M; Tang, Weifeng W; Gu, Haiyong H; Yin, Jun J; Huang, Ziyang Z
Publication Date: 2015

Variant appearance in text: rs3753584
PubMed Link: 26770518
Variant Present in the following documents:
  • Main text
View BVdb publication page



Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study.

Environmental Health Perspectives
Wu, Fen F; Jasmine, Farzana F; Kibriya, Muhammad G MG; Liu, Mengling M; Cheng, Xin X; Parvez, Faruque F; Islam, Tariqul T; Ahmed, Alauddin A; Rakibuz-Zaman, Muhammad M; Jiang, Jieying J; Roy, Shantanu S; Paul-Brutus, Rachelle R; Slavkovich, Vesna V; Islam, Tariqul T; Levy, Diane D; VanderWeele, Tyler J TJ; Pierce, Brandon L BL; Graziano, Joseph H JH; Ahsan, Habibul H; Chen, Yu Y
Publication Date: 2015-05

Variant appearance in text: rs3753584
PubMed Link: 25575156
Variant Present in the following documents:
  • ehp.1307883.s001.508.pdf
View BVdb publication page



Variation in folate pathway genes and distal colorectal adenoma risk: a sigmoidoscopy-based case-control study.

Cancer Causes & Control : Ccc
Levine, A Joan AJ; Lee, Won W; Figueiredo, Jane C JC; Conti, David V DV; Vandenberg, David J DJ; Davis, Brian D BD; Edlund, Christopher K CK; Henning, Susanne M SM; Heber, David D; Stern, Mariana C MC; Haile, Robert W RW
Publication Date: 2011-04

Variant appearance in text: rs3753584
PubMed Link: 21274745
Variant Present in the following documents:
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Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Genetic Epidemiology
Locke, Adam E AE; Dooley, Kenneth J KJ; Tinker, Stuart W SW; Cheong, Soo Yeon SY; Feingold, Eleanor E; Allen, Emily G EG; Freeman, Sallie B SB; Torfs, Claudine P CP; Cua, Clifford L CL; Epstein, Michael P MP; Wu, Michael C MC; Lin, Xihong X; Capone, George G; Sherman, Stephanie L SL; Bean, Lora J H LJ
Publication Date: 2010-09

Variant appearance in text: rs3753584
PubMed Link: 20718043
Variant Present in the following documents:
  • Main text
View BVdb publication page