SBF2 c.55+13546G>C

Variant ID: 11-10302016-C-G

NM_030962.3(SBF2):c.55+13546G>C

This variant was identified in 2 publications

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: rs10500724
PubMed Link: 19039035
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.

Bmc Medical Genetics
O'Donnell, Christopher J CJ; Cupples, L Adrienne LA; D'Agostino, Ralph B RB; Fox, Caroline S CS; Hoffmann, Udo U; Hwang, Shih-Jen SJ; Ingellson, Erik E; Liu, Chunyu C; Murabito, Joanne M JM; Polak, Joseph F JF; Wolf, Philip A PA; Demissie, Serkalem S
Publication Date: 2007-09-19

Variant appearance in text: rs10500724
PubMed Link: 17903303
Variant Present in the following documents:
  • Main text
View BVdb publication page