MTHFR c.587-784G>A

Variant ID: 1-11857240-C-T

NM_005957.4(MTHFR):c.587-784G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs7526128
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
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: rs7526128
PubMed Link: 31882953
Variant Present in the following documents:
  • 41598_2019_56494_MOESM1_ESM.pdf
View BVdb publication page



Genome-wide association study of circulating folate one-carbon metabolites.

Genetic Epidemiology
Wang, Jun J; Asante, Isaac I; Baron, John A JA; Figueiredo, Jane C JC; Haile, Robert R; Joan Levine, A A; Newcomb, Polly A PA; Templeton, Allyson S AS; Schumacher, Fredrick R FR; Louie, Stan G SG; Casey, Graham G; Conti, David V DV
Publication Date: 2019-12

Variant appearance in text: rs7526128
PubMed Link: 31502714
Variant Present in the following documents:
  • Main text
View BVdb publication page