FLNB c.293-5089G>T

Variant ID: 3-58057684-G-T

NM_001457.3(FLNB):c.293-5089G>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Conditional testing of multiple variants associated with bone mineral density in the FLNB gene region suggests that they represent a single association signal.

Bmc Genetics
Mullin, Benjamin H BH; Mamotte, Cyril C; Prince, Richard L RL; Spector, Tim D TD; Dudbridge, Frank F; Wilson, Scott G SG
Publication Date: 2013-10-31

Variant appearance in text: rs9822918
PubMed Link: 24176111
Variant Present in the following documents:
  • Main text
  • 1471-2156-14-107.pdf
View BVdb publication page



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: rs9822918
PubMed Link: 20357209
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants in FLNB/CRTAP, not ARHGEF3 at 3p, are associated with osteoporosis in southern Chinese women.

Osteoporosis International : A Journal Established As Result Of Cooperation Between The European Foundation For Osteoporosis And The National Osteoporosis Foundation Of The Usa
Li, G H Y GH; Kung, A W C AW; Huang, Q-Y QY
Publication Date: 2010-06

Variant appearance in text: rs9822918
PubMed Link: 19727905
Variant Present in the following documents:
  • Main text
  • 198_2009_Article_1043.pdf
View BVdb publication page