THSD7A c.1822+12516C>T

Variant ID: 7-11568530-G-A

NM_015204.2(THSD7A):c.1822+12516C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Molecular genetic studies of gene identification for osteoporosis: the 2009 update.

Endocrine Reviews
Xu, Xiang-Hong XH; Dong, Shan-Shan SS; Guo, Yan Y; Yang, Tie-Lin TL; Lei, Shu-Feng SF; Papasian, Christopher J CJ; Zhao, Ming M; Deng, Hong-Wen HW
Publication Date: 2010-08

Variant appearance in text: rs12673692
PubMed Link: 20357209
Variant Present in the following documents:
  • Main text
View BVdb publication page