RORA c.167-231972T>G

Variant ID: 15-61202857-A-C

NM_134261.2(RORA):c.167-231972T>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Circadian clock-related genetic risk scores and risk of placental abruption.

Placenta
Qiu, Chunfang C; Gelaye, Bizu B; Denis, Marie M; Tadesse, Mahlet G MG; Luque Fernandez, Miguel Angel MA; Enquobahrie, Daniel A DA; Ananth, Cande V CV; Sanchez, Sixto E SE; Williams, Michelle A MA
Publication Date: 2015-12

Variant appearance in text: rs8042228
PubMed Link: 26515929
Variant Present in the following documents:
  • Main text
View BVdb publication page



Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.

Molecular Vision
Ravesh, Zeinab Z; El Asrag, Mohammed E ME; Weisschuh, Nicole N; McKibbin, Martin M; Reuter, Peggy P; Watson, Christopher M CM; Baumann, Britta B; Poulter, James A JA; Sajid, Sundus S; Panagiotou, Evangelia S ES; O'Sullivan, James J; Abdelhamed, Zakia Z; Bonin, Michael M; Soltanifar, Mehdi M; Black, Graeme C M GC; Amin-ud Din, Muhammad M; Toomes, Carmel C; Ansar, Muhammad M; Inglehearn, Chris F CF; Wissinger, Bernd B; Ali, Manir M
Publication Date: 2015

Variant appearance in text: rs8042228
PubMed Link: 25802487
Variant Present in the following documents:
  • Main text
  • mv-v21-236.pdf
View BVdb publication page