RARA c.178+1522A>G

Variant ID: 17-38489170-A-G

NM_000964.3(RARA):c.178+1522A>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: rs2715554
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
View BVdb publication page



The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measures.

Molecular Vision
Veerappan, S S; Schäche, M M; Pertile, K K KK; Islam, F M A FM; Chen, C Y CY; Mitchell, P P; Dirani, M M; Baird, P N PN
Publication Date: 2009-07-17

Variant appearance in text: rs2715554
PubMed Link: 19626135
Variant Present in the following documents:
  • Main text
  • mv-v15-1390.pdf
View BVdb publication page