CEACAM6 c.424+2024G>A

Variant ID: 19-42262891-G-A

NM_002483.4(CEACAM6):c.424+2024G>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: rs3795020
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



CEACAM6 gene variants in inflammatory bowel disease.

Plos One
Glas, Jürgen J; Seiderer, Julia J; Fries, Christoph C; Tillack, Cornelia C; Pfennig, Simone S; Weidinger, Maria M; Beigel, Florian F; Olszak, Torsten T; Lass, Ulrich U; Göke, Burkhard B; Ochsenkühn, Thomas T; Wolf, Christiane C; Lohse, Peter P; Müller-Myhsok, Bertram B; Diegelmann, Julia J; Czamara, Darina D; Brand, Stephan S
Publication Date: 2011-04-29

Variant appearance in text: rs3795020
PubMed Link: 21559399
Variant Present in the following documents:
  • Main text
  • pone.0019319.pdf
View BVdb publication page