RARA c.179-3654T>C

Variant ID: 17-38500914-T-C

NM_000964.3(RARA):c.179-3654T>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.

Acta Neuropathologica Communications
Shankar, Ganesh M GM; Taylor-Weiner, Amaro A; Lelic, Nina N; Jones, Robert T RT; Kim, James C JC; Francis, Joshua M JM; Abedalthagafi, Malak M; Borges, Lawrence F LF; Coumans, Jean-Valery JV; Curry, William T WT; Nahed, Brian V BV; Shin, John H JH; Paek, Sun Ha SH; Park, Sung-Hye SH; Stewart, Chip C; Lawrence, Michael S MS; Cibulskis, Kristian K; Thorner, Aaron R AR; Van Hummelen, Paul P; Stemmer-Rachamimov, Anat O AO; Batchelor, Tracy T TT; Carter, Scott L SL; Hoang, Mai P MP; Santagata, Sandro S; Louis, David N DN; Barker, Fred G FG; Meyerson, Matthew M; Getz, Gad G; Brastianos, Priscilla K PK; Cahill, Daniel P DP
Publication Date: 2014-12-24

Variant appearance in text: rs9303285
PubMed Link: 25589003
Variant Present in the following documents:
  • 40478_2014_167_MOESM1_ESM.xlsx, sheet 6
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: rs9303285
PubMed Link: 19626135
Variant Present in the following documents:
  • Main text
  • mv-v15-1390.pdf
View BVdb publication page