ARHGAP17 c.1333+369T>C

Variant ID: 16-24954723-A-G

NM_001006634.1(ARHGAP17):c.1333+369T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association study identifies common variants associated with circulating vitamin E levels.

Human Molecular Genetics
Major, Jacqueline M JM; Yu, Kai K; Wheeler, William W; Zhang, Hong H; Cornelis, Marilyn C MC; Wright, Margaret E ME; Yeager, Meredith M; Snyder, Kirk K; Weinstein, Stephanie J SJ; Mondul, Alison A; Eliassen, Heather H; Purdue, Mark M; Hazra, Aditi A; McCarty, Catherine A CA; Hendrickson, Sara S; Virtamo, Jarmo J; Hunter, David D; Chanock, Stephen S; Kraft, Peter P; Albanes, Demetrius D
Publication Date: 2011-10-01

Variant appearance in text: rs3815951
PubMed Link: 21729881
Variant Present in the following documents:
  • Main text
  • ddr296.pdf
View BVdb publication page