ST3GAL4 c.-61+17912C>T

Variant ID: 11-126243649-C-T

NM_001254757.2(ST3GAL4):c.-61+17912C>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: rs3862630
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections.

Nature Communications
Tian, Chao C; Hromatka, Bethann S BS; Kiefer, Amy K AK; Eriksson, Nicholas N; Noble, Suzanne M SM; Tung, Joyce Y JY; Hinds, David A DA
Publication Date: 2017-09-19

Variant appearance in text: rs3862630
PubMed Link: 28928442
Variant Present in the following documents:
  • Main text
  • 41467_2017_Article_257.pdf
  • 41467_2017_257_MOESM1_ESM.pdf
View BVdb publication page