MTRR c.1146+640C>T

Variant ID: 5-7887456-C-T

NM_002454.2(MTRR):c.1146+640C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs162039
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page



Obstructive heart defects associated with candidate genes, maternal obesity, and folic acid supplementation.

American Journal Of Medical Genetics. Part A
Tang, Xinyu X; Cleves, Mario A MA; Nick, Todd G TG; Li, Ming M; MacLeod, Stewart L SL; Erickson, Stephen W SW; Li, Jingyun J; Shaw, Gary M GM; Mosley, Bridget S BS; Hobbs, Charlotte A CA; ,
Publication Date: 2015-06

Variant appearance in text: rs162039
PubMed Link: 25846410
Variant Present in the following documents:
  • Main text
View BVdb publication page



A case-parent triad assessment of folate metabolic genes and the risk of childhood acute lymphoblastic leukemia.

Cancer Causes & Control : Ccc
Lupo, Philip J PJ; Nousome, Darryl D; Kamdar, Kala Y KY; Okcu, M Fatih MF; Scheurer, Michael E ME
Publication Date: 2012-11

Variant appearance in text: rs162039
PubMed Link: 22941668
Variant Present in the following documents:
  • Main text
View BVdb publication page