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