FLNB c.292+12169C>T

Variant ID: 3-58006752-C-T

NM_001457.3(FLNB):c.292+12169C>T

This variant was identified in 1 publication

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: rs7634753
PubMed Link: 24176111
Variant Present in the following documents:
  • Main text
  • 1471-2156-14-107.pdf
View BVdb publication page