MTHFD1 c.2458-2060A>G

Variant ID: 14-64918412-A-G

NM_005956.3(MTHFD1):c.2458-2060A>G

This variant was identified in 7 publications

View GRCh38 version.




Publications:


Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study.

Bmc Pregnancy And Childbirth
Song, Xinli X; Li, Qiongxuan Q; Diao, Jingyi J; Li, Jinqi J; Li, Yihuan Y; Zhang, Senmao S; Zhao, Lijuan L; Chen, Letao L; Wei, Jianhui J; Shu, Jing J; Liu, Yiping Y; Sun, Mengting M; Huang, Peng P; Wang, Tingting T; Qin, Jiabi J
Publication Date: 2022-01-31

Variant appearance in text: rs11849530
PubMed Link: 35100977
Variant Present in the following documents:
  • Main text
  • 12884_2022_Article_4419.pdf
View BVdb publication page



Association of MTHFD1 gene polymorphisms and maternal smoking with risk of congenital heart disease: a hospital-based case-control study.

Bmc Pregnancy And Childbirth
Song, Xinli X; Li, Qiongxuan Q; Diao, Jingyi J; Li, Jinqi J; Li, Yihuan Y; Zhang, Senmao S; Zhao, Lijuan L; Chen, Letao L; Wei, Jianhui J; Shu, Jing J; Liu, Yiping Y; Sun, Mengting M; Huang, Peng P; Wang, Tingting T; Qin, Jiabi J
Publication Date: 2022-01-31

Variant appearance in text: rs11849530
PubMed Link: 35100977
Variant Present in the following documents:
  • Main text
  • 12884_2022_Article_4419.pdf
View BVdb publication page



Maternal and infant gene-folate interactions and the risk of neural tube defects.

American Journal Of Medical Genetics. Part A
Etheredge, Analee J AJ; Finnell, Richard H RH; Carmichael, Suzan L SL; Lammer, Edward J EJ; Zhu, Huiping H; Mitchell, Laura E LE; Shaw, Gary M GM
Publication Date: 2012-10

Variant appearance in text: rs11849530
PubMed Link: 22903727
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene variants in the folate-mediated one-carbon metabolism (FOCM) pathway as risk factors for conotruncal heart defects.

American Journal Of Medical Genetics. Part A
Zhu, Huiping H; Yang, Wei W; Lu, Wei W; Etheredge, Analee J AJ; Lammer, Edward J EJ; Finnell, Richard H RH; Carmichael, Suzan L SL; Shaw, Gary M GM
Publication Date: 2012-05

Variant appearance in text: rs11849530
PubMed Link: 22495907
Variant Present in the following documents:
  • Main text
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: rs11849530
PubMed Link: 21274745
Variant Present in the following documents:
View BVdb publication page



Folate pathway and nonsyndromic cleft lip and palate.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Blanton, Susan H SH; Henry, Robin R RR; Yuan, Quiping Q; Mulliken, John B JB; Stal, Samuel S; Finnell, Richard H RH; Hecht, Jacqueline T JT
Publication Date: 2011-01

Variant appearance in text: rs11849530
PubMed Link: 21254359
Variant Present in the following documents:
  • Main text
View BVdb publication page



Nonsyndromic cleft lip and palate: CRISPLD genes and the folate gene pathway connection.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Chiquet, Brett T BT; Henry, Robin R; Burt, Amber A; Mulliken, John B JB; Stal, Samuel S; Blanton, Susan H SH; Hecht, Jacqueline T JT
Publication Date: 2011-01

Variant appearance in text: rs11849530
PubMed Link: 21254358
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: rs11849530
PubMed Link: 19493349
Variant Present in the following documents:
  • Main text
  • 1471-2350-10-49.pdf
View BVdb publication page