RUNX1 c.613+9632A>T

Variant ID: 21-36222139-T-A

NM_001754.4(RUNX1):c.613+9632A>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


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: rs8134380
PubMed Link: 21088106
Variant Present in the following documents:
  • Main text
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