FLNB c.292+14676G>T

Variant ID: 3-58009259-G-T

NM_001457.3(FLNB):c.292+14676G>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.

Human Molecular Genetics
Lei, Shu-Feng SF; Tan, Li-Jun LJ; Liu, Xiao-Gang XG; Wang, Liang L; Yan, Han H; Guo, Yan-Fang YF; Liu, Yao-Zhong YZ; Xiong, Dong-Hai DH; Li, Jian J; Yang, Tie-Lin TL; Chen, Xiang-Ding XD; Guo, Yan Y; Deng, Fei-Yan FY; Zhang, Yin-Ping YP; Zhu, Xue-Zhen XZ; Levy, Shawn S; Papasian, Christopher J CJ; Hamilton, James J JJ; Recker, Robert R RR; Deng, Hong-Wen HW
Publication Date: 2009-05-01

Variant appearance in text: rs1658342
PubMed Link: 19039035
Variant Present in the following documents:
  • Main text
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