SLC2A3 c.15+389A>G

Variant ID: 12-8088227-T-C

NM_006931.2(SLC2A3):c.15+389A>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: rs2244822
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



Novel insights into the regulatory architecture of CD4+ T cells in rheumatoid arthritis.

Plos One
Aterido, AdriĆ  A; Palacio, Carlos C; Marsal, Sara S; Avila, Gabriela G; JuliĆ , Antonio A
Publication Date: 2014

Variant appearance in text: rs2244822
PubMed Link: 24959711
Variant Present in the following documents:
  • Main text
  • pone.0100690.pdf
View BVdb publication page