RFC1 c.3+3171G>T

Variant ID: 4-39364688-C-A

NM_002913.4(RFC1):c.3+3171G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Conotruncal heart defects and common variants in maternal and fetal genes in folate, homocysteine, and transsulfuration pathways.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Hobbs, Charlotte A CA; Cleves, Mario A MA; Macleod, Stewart L SL; Erickson, Stephen W SW; Tang, Xinyu X; Li, Jingyun J; Li, Ming M; Nick, Todd T; Malik, Sadia S; ,
Publication Date: 2014-02

Variant appearance in text: rs16995255
PubMed Link: 24535845
Variant Present in the following documents:
  • Main text
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