BHMT c.33+1655T>C

Variant ID: 5-78409396-T-C

NM_001713.2(BHMT):c.33+1655T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Genetic Susceptibility to Drug Teratogenicity: A Systematic Literature Review.

Frontiers In Genetics
Gomes, Julia do Amaral JDA; Olstad, Emilie Willoch EW; Kowalski, Thayne Woycinck TW; Gervin, Kristina K; Vianna, Fernanda Sales Luiz FSL; Schüler-Faccini, Lavínia L; Nordeng, Hedvig Marie Egeland HME
Publication Date: 2021

Variant appearance in text: rs542852
PubMed Link: 33981330
Variant Present in the following documents:
  • Main text
View BVdb publication page



Maternal and infant genetic variants, maternal periconceptional use of selective serotonin reuptake inhibitors, and risk of congenital heart defects in offspring: population based study.

Bmj (Clinical Research Ed.)
Nembhard, Wendy N WN; Tang, Xinyu X; Hu, Zhuopei Z; MacLeod, Stewart S; Stowe, Zachary Z; Webber, Daniel D; ,
Publication Date: 2017-03-06

Variant appearance in text: rs542852
PubMed Link: 28264803
Variant Present in the following documents:
  • Main text
View BVdb publication page



Betaine-homocysteine methyltransferase: human liver genotype-phenotype correlation.

Molecular Genetics And Metabolism
Feng, Qiping Q; Kalari, Krishna K; Fridley, Brooke L BL; Jenkins, Gregory G; Ji, Yuan Y; Abo, Ryan R; Hebbring, Scott S; Zhang, Jianping J; Nye, Monica D MD; Leeder, J Steven JS; Weinshilboum, Richard M RM
Publication Date: 2011-02

Variant appearance in text: rs542852
PubMed Link: 21093336
Variant Present in the following documents:
  • Main text
View BVdb publication page