IGF2R c.150-9511G>A

Variant ID: 6-160402705-G-A

NM_000876.2(IGF2R):c.150-9511G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Signals of recent positive selection in a worldwide sample of human populations.

Genome Research
Pickrell, Joseph K JK; Coop, Graham G; Novembre, John J; Kudaravalli, Sridhar S; Li, Jun Z JZ; Absher, Devin D; Srinivasan, Balaji S BS; Barsh, Gregory S GS; Myers, Richard M RM; Feldman, Marcus W MW; Pritchard, Jonathan K JK
Publication Date: 2009-05

Variant appearance in text: rs6917747
PubMed Link: 19307593
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.

Human Molecular Genetics
Baranzini, Sergio E SE; Wang, Joanne J; Gibson, Rachel A RA; Galwey, Nicholas N; Naegelin, Yvonne Y; Barkhof, Frederik F; Radue, Ernst-Wilhelm EW; Lindberg, Raija L P RL; Uitdehaag, Bernard M G BM; Johnson, Michael R MR; Angelakopoulou, Aspasia A; Hall, Leslie L; Richardson, Jill C JC; Prinjha, Rab K RK; Gass, Achim A; Geurts, Jeroen J G JJ; Kragt, Jolijn J; Sombekke, Madeleine M; Vrenken, Hugo H; Qualley, Pamela P; Lincoln, Robin R RR; Gomez, Refujia R; Caillier, Stacy J SJ; George, Michaela F MF; Mousavi, Hourieh H; Guerrero, Rosa R; Okuda, Darin T DT; Cree, Bruce A C BA; Green, Ari J AJ; Waubant, Emmanuelle E; Goodin, Douglas S DS; Pelletier, Daniel D; Matthews, Paul M PM; Hauser, Stephen L SL; Kappos, Ludwig L; Polman, Chris H CH; Oksenberg, Jorge R JR
Publication Date: 2009-02-15

Variant appearance in text: rs6917747
PubMed Link: 19010793
Variant Present in the following documents:
  • Main text
View BVdb publication page