RFX6 c.2611+1117C>T

Variant ID: 6-117251251-C-T

NM_173560.3(RFX6):c.2611+1117C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites.

Human Mutation
Bu, Huajie H; Narisu, Narisu N; Schlick, Bettina B; Rainer, Johannes J; Manke, Thomas T; Schäfer, Georg G; Pasqualini, Lorenza L; Chines, Peter P; Schweiger, Michal R MR; Fuchsberger, Christian C; Klocker, Helmut H
Publication Date: 2016-01

Variant appearance in text: rs657963
PubMed Link: 26411452
Variant Present in the following documents:
  • HUMU-37-52-s001.pdf
View BVdb publication page