RARG c.184+3317T>C

Variant ID: 12-53617829-A-G

NM_000966.5(RARG):c.184+3317T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Chiari malformation type I: a case-control association study of 58 developmental genes.

Plos One
Urbizu, Aintzane A; Toma, Claudio C; Poca, Maria A MA; Sahuquillo, Juan J; Cuenca-León, Ester E; Cormand, Bru B; Macaya, Alfons A
Publication Date: 2013

Variant appearance in text: rs6580936
PubMed Link: 23437350
Variant Present in the following documents:
  • Main text
  • pone.0057241.pdf
View BVdb publication page



Association of retinoic acid receptor genes with meningomyelocele.

Birth Defects Research. Part A, Clinical And Molecular Teratology
Tran, Phong X PX; Au, Kit Sing KS; Morrison, Alanna C AC; Fletcher, Jack M JM; Ostermaier, Kathryn K KK; Tyerman, Gayle H GH; Northrup, Hope H
Publication Date: 2011-01

Variant appearance in text: rs6580936
PubMed Link: 21254357
Variant Present in the following documents:
  • Main text
View BVdb publication page