CDKAL1 c.286+21103C>T

Variant ID: 6-20570039-C-T

NM_017774.3(CDKAL1):c.286+21103C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Selecting cases and controls for DNA sequencing studies using family histories of disease.

Statistics In Medicine
Kim, Wonji W; Qiao, Dandi D; Cho, Michael H MH; Kwak, Soo Heon SH; Park, Kyong Soo KS; Silverman, Edwin K EK; Sham, Pak P; Won, Sungho S
Publication Date: 2017-06-15

Variant appearance in text: rs4291090
PubMed Link: 28222494
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene and pathway-based second-wave analysis of genome-wide association studies.

European Journal Of Human Genetics : Ejhg
Peng, Gang G; Luo, Li L; Siu, Hoicheong H; Zhu, Yun Y; Hu, Pengfei P; Hong, Shengjun S; Zhao, Jinying J; Zhou, Xiaodong X; Reveille, John D JD; Jin, Li L; Amos, Christopher I CI; Xiong, Momiao M
Publication Date: 2010-01

Variant appearance in text: rs4291090
PubMed Link: 19584899
Variant Present in the following documents:
  • Main text
View BVdb publication page