RARB c.158-7047C>G

Variant ID: 3-25495637-C-G

NM_000965.3(RARB):c.158-7047C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs13314219
PubMed Link: 21254357
Variant Present in the following documents:
  • Main text
View BVdb publication page