CAT c.67-2100A>T

Variant ID: 11-34468639-A-T

NM_001752.3(CAT):c.67-2100A>T

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: rs560807
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Association of genetic variants with diabetic nephropathy.

World Journal Of Diabetes
Rizvi, Saliha S; Raza, Syed Tasleem ST; Mahdi, Farzana F
Publication Date: 2014-12-15

Variant appearance in text: rs560807
PubMed Link: 25512783
Variant Present in the following documents:
  • Main text
View BVdb publication page