RUNX1 c.509-281G>A

Variant ID: 21-36232156-C-T

NM_001754.4(RUNX1):c.509-281G>A

This variant was identified in 3 publications

View GRCh38 version.




Publications:


A pathway approach to evaluating the association between the CHIEF pathway and risk of colorectal cancer.

Carcinogenesis
Slattery, Martha L ML; Wolff, Roger K RK; Lundgreen, Abbie A
Publication Date: 2015-01

Variant appearance in text: rs2248720
PubMed Link: 25330801
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between genetic variation in RUNX1, RUNX2, RUNX3, MAPK1 and eIF4E and riskof colon and rectal cancer: additional support for a TGF-β-signaling pathway.

Carcinogenesis
Slattery, Martha L ML; Lundgreen, Abbie A; Herrick, Jennifer S JS; Caan, Bette J BJ; Potter, John D JD; Wolff, Roger K RK
Publication Date: 2011-03

Variant appearance in text: rs2248720
PubMed Link: 21088106
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver disease.

Gastroenterology
Roberts, Kari E KE; Kawut, Steven M SM; Krowka, Michael J MJ; Brown, Robert S RS; Trotter, James F JF; Shah, Vijay V; Peter, Inga I; Tighiouart, Hocine H; Mitra, Nandita N; Handorf, Elizabeth E; Knowles, James A JA; Zacks, Steven S; Fallon, Michael B MB; ,
Publication Date: 2010-07

Variant appearance in text: rs2248720
PubMed Link: 20346360
Variant Present in the following documents:
  • Main text
View BVdb publication page