RARB c.306+8023G>C

Variant ID: 3-25510855-G-C

NM_000965.3(RARB):c.306+8023G>C

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: rs4681064
PubMed Link: 21254357
Variant Present in the following documents:
  • Main text
View BVdb publication page