MTHFR c.-13-788G>A

Variant ID: 1-11863974-C-T

NM_005957.4(MTHFR):c.-13-788G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association analysis of maternal MTHFR gene polymorphisms and the occurrence of congenital heart disease in offspring.

Bmc Cardiovascular Disorders
Sun, Mengting M; Wang, Tingting T; Huang, Peng P; Diao, Jingyi J; Zhang, Senmao S; Li, Jinqi J; Luo, Liu L; Li, Yihuan Y; Chen, Letao L; Liu, Yiping Y; Wei, Jianhui J; Song, Xinli X; Sheng, Xiaoqi X; Qin, Jiabi J
Publication Date: 2021-06-14

Variant appearance in text: rs1931226
PubMed Link: 34126931
Variant Present in the following documents:
  • Main text
  • 12872_2021_Article_2117.pdf
View BVdb publication page



Haplotype analysis of the folate-related genes MTHFR, MTRR, and MTR and migraine with aura.

Cephalalgia : An International Journal Of Headache
Roecklein, Kathryn A KA; Scher, Ann I AI; Smith, Albert A; Harris, Tamara T; Eiriksdottir, Gudny G; Garcia, Melissa M; Gudnason, Villi V; Launer, Lenore J LJ
Publication Date: 2013-05

Variant appearance in text: rs1931226
PubMed Link: 23430981
Variant Present in the following documents:
  • Main text
View BVdb publication page



118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects.

Bmc Medical Genetics
Shaw, Gary M GM; Lu, Wei W; Zhu, Huiping H; Yang, Wei W; Briggs, Farren B S FB; Carmichael, Suzan L SL; Barcellos, Lisa F LF; Lammer, Edward J EJ; Finnell, Richard H RH
Publication Date: 2009-06-03

Variant appearance in text: rs1931226
PubMed Link: 19493349
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-49.pdf
View BVdb publication page