GPHN c.2079+2702C>T

Variant ID: 14-67638455-C-T

NM_020806.4(GPHN):c.2079+2702C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide SNP typing reveals signatures of population history.

Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07

Variant appearance in text: rs2281676
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
View BVdb publication page