RORA c.166+20900C>G

Variant ID: 15-61500352-G-C

NM_134261.2(RORA):c.166+20900C>G

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts.

Nature Communications
Rashkin, Sara R SR; Graff, Rebecca E RE; Kachuri, Linda L; Thai, Khanh K KK; Alexeeff, Stacey E SE; Blatchins, Maruta A MA; Cavazos, Taylor B TB; Corley, Douglas A DA; Emami, Nima C NC; Hoffman, Joshua D JD; Jorgenson, Eric E; Kushi, Lawrence H LH; Meyers, Travis J TJ; Van Den Eeden, Stephen K SK; Ziv, Elad E; Habel, Laurel A LA; Hoffmann, Thomas J TJ; Sakoda, Lori C LC; Witte, John S JS
Publication Date: 2020-09-04

Variant appearance in text: rs112248293
PubMed Link: 32887889
Variant Present in the following documents:
  • Main text
  • 41467_2020_Article_18246.pdf
View BVdb publication page