PCSK2 c.710-340A>G

Variant ID: 20-17417013-A-G

NM_002594.3(PCSK2):c.710-340A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs890609
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



Genetic polymorphisms of PCSK2 are associated with glucose homeostasis and progression to type 2 diabetes in a Chinese population.

Scientific Reports
Chang, Tien-Jyun TJ; Chiu, Yen-Feng YF; Sheu, Wayne H-H WH; Shih, Kuang-Chung KC; Hwu, Chii-Min CM; Quertermous, Thomas T; Jou, Yuh-Shan YS; Kuo, Shan-Shan SS; Chang, Yi-Cheng YC; Chuang, Lee-Ming LM
Publication Date: 2015-11-26

Variant appearance in text: rs890609
PubMed Link: 26607656
Variant Present in the following documents:
  • Main text
  • srep14380.pdf
View BVdb publication page