CDKAL1 c.287-17571C>A

Variant ID: 6-20631953-C-A

NM_017774.3(CDKAL1):c.287-17571C>A

This variant was identified in 3 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: rs2328529
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: rs2328529
PubMed Link: 19584899
Variant Present in the following documents:
  • Main text
View BVdb publication page



Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.

Diabetes
Takeuchi, Fumihiko F; Serizawa, Masakuni M; Yamamoto, Ken K; Fujisawa, Tomomi T; Nakashima, Eitaro E; Ohnaka, Keizo K; Ikegami, Hiroshi H; Sugiyama, Takao T; Katsuya, Tomohiro T; Miyagishi, Makoto M; Nakashima, Naoki N; Nawata, Hajime H; Nakamura, Jiro J; Kono, Suminori S; Takayanagi, Ryoichi R; Kato, Norihiro N
Publication Date: 2009-07

Variant appearance in text: rs2328529
PubMed Link: 19401414
Variant Present in the following documents:
  • supp_db08-1494_db08-1494_online_appendix.pdf
View BVdb publication page