CSMD1 c.302+53107C>T

Variant ID: 8-4441757-G-A

NM_033225.5(CSMD1):c.302+53107C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


A multi-stage genome-wide association study of uterine fibroids in African Americans.

Human Genetics
Hellwege, Jacklyn N JN; Jeff, Janina M JM; Wise, Lauren A LA; Gallagher, C Scott CS; Wellons, Melissa M; Hartmann, Katherine E KE; Jones, Sarah F SF; Torstenson, Eric S ES; Dickinson, Scott S; Ruiz-Narváez, Edward A EA; Rohland, Nadin N; Allen, Alexander A; Reich, David D; Tandon, Arti A; Pasaniuc, Bogdan B; Mancuso, Nicholas N; Im, Hae Kyung HK; Hinds, David A DA; Palmer, Julie R JR; Rosenberg, Lynn L; Denny, Joshua C JC; Roden, Dan M DM; Stewart, Elizabeth A EA; Morton, Cynthia C CC; Kenny, Eimear E EE; Edwards, Todd L TL; Velez Edwards, Digna R DR
Publication Date: 2017-10

Variant appearance in text: rs11987636
PubMed Link: 28836065
Variant Present in the following documents:
  • Main text
  • 439_2017_Article_1836.pdf
View BVdb publication page