PROX2 c.1609-322T>G

Variant ID: 14-75322327-A-C

NM_001243007.1(PROX2):c.1609-322T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Functional annotation of structural ncRNAs within enhancer RNAs in the human genome: implications for human disease.

Scientific Reports
Ren, Chao C; Liu, Feng F; Ouyang, Zhangyi Z; An, Gaole G; Zhao, Chenghui C; Shuai, Jun J; Cai, Shuhong S; Bo, Xiaochen X; Shu, Wenjie W
Publication Date: 2017-11-14

Variant appearance in text: rs10483863
PubMed Link: 29138457
Variant Present in the following documents:
  • 41598_2017_15822_MOESM8_ESM.xlsx, sheet 3
  • 41598_2017_15822_MOESM8_ESM.xlsx, sheet 4
View BVdb publication page



The efficacy of detecting variants with small effects on the Affymetrix 6.0 platform using pooled DNA.

Human Genetics
Chiang, Charleston W K CW; Gajdos, Zofia K Z ZK; Korn, Joshua M JM; Butler, Johannah L JL; Hackett, Rachel R; Guiducci, Candace C; Nguyen, Thutrang T TT; Wilks, Rainford R; Forrester, Terrence T; Henderson, Katherine D KD; Le Marchand, Loic L; Henderson, Brian E BE; Haiman, Christopher A CA; Cooper, Richard S RS; Lyon, Helen N HN; Zhu, Xiaofeng X; McKenzie, Colin A CA; Palmert, Mark R MR; Hirschhorn, Joel N JN
Publication Date: 2011-11

Variant appearance in text: rs10483863
PubMed Link: 21424828
Variant Present in the following documents:
  • Main text
View BVdb publication page