FBN1 c.1714+306G>A

Variant ID: 15-48801935-C-T

NM_000138.4(FBN1):c.1714+306G>A

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

Nature Communications
Iglesias, Adriana I AI; Mishra, Aniket A; Vitart, Veronique V; Bykhovskaya, Yelena Y; Höhn, René R; Springelkamp, Henriët H; Cuellar-Partida, Gabriel G; Gharahkhani, Puya P; Bailey, Jessica N Cooke JNC; Willoughby, Colin E CE; Li, Xiaohui X; Yazar, Seyhan S; Nag, Abhishek A; Khawaja, Anthony P AP; Polašek, Ozren O; Siscovick, David D; Mitchell, Paul P; Tham, Yih Chung YC; Haines, Jonathan L JL; Kearns, Lisa S LS; Hayward, Caroline C; Shi, Yuan Y; van Leeuwen, Elisabeth M EM; Taylor, Kent D KD; , ; Bonnemaijer, Pieter P; Rotter, Jerome I JI; Martin, Nicholas G NG; Zeller, Tanja T; Mills, Richard A RA; Souzeau, Emmanuelle E; Staffieri, Sandra E SE; Jonas, Jost B JB; Schmidtmann, Irene I; Boutin, Thibaud T; Kang, Jae H JH; Lucas, Sionne E M SEM; Wong, Tien Yin TY; Beutel, Manfred E ME; Wilson, James F JF; , ; , ; Uitterlinden, André G AG; Vithana, Eranga N EN; Foster, Paul J PJ; Hysi, Pirro G PG; Hewitt, Alex W AW; Khor, Chiea Chuen CC; Pasquale, Louis R LR; Montgomery, Grant W GW; Klaver, Caroline C W CCW; Aung, Tin T; Pfeiffer, Norbert N; Mackey, David A DA; Hammond, Christopher J CJ; Cheng, Ching-Yu CY; Craig, Jamie E JE; Rabinowitz, Yaron S YS; Wiggs, Janey L JL; Burdon, Kathryn P KP; van Duijn, Cornelia M CM; MacGregor, Stuart S
Publication Date: 2018-05-14

Variant appearance in text: rs8030753
PubMed Link: 29760442
Variant Present in the following documents:
  • Main text
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