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RUNX2 c.58+13223A>C
Variant ID: 6-45309744-A-C
NM_001024630.3(
RUNX2
):c.58+13223A>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:
Calcium Signaling Pathway Genes RUNX2 and CACNA1C Are Associated With Calcific Aortic Valve Disease.
Circulation. Cardiovascular Genetics
Guauque-Olarte, Sandra S; Messika-Zeitoun, David D; Droit, Arnaud A; Lamontagne, Maxime M; Tremblay-Marchand, Joël J; Lavoie-Charland, Emilie E; Gaudreault, Nathalie N; Arsenault, Benoit J BJ; Dubé, Marie-Pierre MP; Tardif, Jean-Claude JC; Body, Simon C SC; Seidman, Jonathan G JG; Boileau, Catherine C; Mathieu, Patrick P; Pibarot, Philippe P; Bossé, Yohan Y
Publication Date: 2015-12
Variant appearance in text: rs144071310
PubMed Link:
26553695
Variant Present in the following documents:
Main text
View BVdb publication page