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RARB c.306+4198A>G
Variant ID: 3-25507030-A-G
NM_000965.3(
RARB
):c.306+4198A>G
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: rs6778350
PubMed Link:
21254357
Variant Present in the following documents:
Main text
View BVdb publication page