CELSR2 c.8054+106G>A

Variant ID: 1-109815133-G-A

NM_001408.2(CELSR2):c.8054+106G>A

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: rs79482788
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Inference of a causal relation between low-density lipoprotein cholesterol and hypertension using mendelian randomization analysis.

Clinical Hypertension
Go, Tae-Hwa TH; Kwak, Kyeong Im KI; Jang, Ji-Yun JY; Yu, Minheui M; Kim, Hye Sim HS; Kim, Jang Young JY; Koh, Sang Baek SB; Kang, Dae Ryong DR
Publication Date: 2021-02-26

Variant appearance in text: rs79482788
PubMed Link: 33637130
Variant Present in the following documents:
  • Main text
  • 40885_2021_Article_162.pdf
View BVdb publication page