MTRR c.401+800T>C

Variant ID: 5-7876288-T-C

NM_002454.2(MTRR):c.401+800T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Genetic Epidemiology
Locke, Adam E AE; Dooley, Kenneth J KJ; Tinker, Stuart W SW; Cheong, Soo Yeon SY; Feingold, Eleanor E; Allen, Emily G EG; Freeman, Sallie B SB; Torfs, Claudine P CP; Cua, Clifford L CL; Epstein, Michael P MP; Wu, Michael C MC; Lin, Xihong X; Capone, George G; Sherman, Stephanie L SL; Bean, Lora J H LJ
Publication Date: 2010-09

Variant appearance in text: rs326121
PubMed Link: 20718043
Variant Present in the following documents:
  • Main text
View BVdb publication page