CR1L c.97+4486T>A

Variant ID: 1-207823161-T-A

NM_175710.1(CR1L):c.97+4486T>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease.

Molecular Psychiatry
Lambert, J-C JC; Grenier-Boley, B B; Harold, D D; Zelenika, D D; Chouraki, V V; Kamatani, Y Y; Sleegers, K K; Ikram, M A MA; Hiltunen, M M; Reitz, C C; Mateo, I I; Feulner, T T; Bullido, M M; Galimberti, D D; Concari, L L; Alvarez, V V; Sims, R R; Gerrish, A A; Chapman, J J; Deniz-Naranjo, C C; Solfrizzi, V V; Sorbi, S S; Arosio, B B; Spalletta, G G; Siciliano, G G; Epelbaum, J J; Hannequin, D D; Dartigues, J-F JF; Tzourio, C C; Berr, C C; Schrijvers, E M C EM; Rogers, R R; Tosto, G G; Pasquier, F F; Bettens, K K; Van Cauwenberghe, C C; Fratiglioni, L L; Graff, C C; Delepine, M M; Ferri, R R; Reynolds, C A CA; Lannfelt, L L; Ingelsson, M M; Prince, J A JA; Chillotti, C C; Pilotto, A A; Seripa, D D; Boland, A A; Mancuso, M M; Bossù, P P; Annoni, G G; Nacmias, B B; Bosco, P P; Panza, F F; Sanchez-Garcia, F F; Del Zompo, M M; Coto, E E; Owen, M M; O'Donovan, M M; Valdivieso, F F; Caffarra, P P; Caffara, P P; Scarpini, E E; Combarros, O O; Buée, L L; Campion, D D; Soininen, H H; Breteler, M M; Riemenschneider, M M; Van Broeckhoven, C C; Alpérovitch, A A; Lathrop, M M; Trégouët, D-A DA; Williams, J J; Amouyel, P P
Publication Date: 2013-04

Variant appearance in text: rs1323720
PubMed Link: 22430674
Variant Present in the following documents:
  • Main text
  • mp201214a.pdf
View BVdb publication page



Integrating pathway analysis and genetics of gene expression for genome-wide association studies.

American Journal Of Human Genetics
Zhong, Hua H; Yang, Xia X; Kaplan, Lee M LM; Molony, Cliona C; Schadt, Eric E EE
Publication Date: 2010-04-09

Variant appearance in text: rs1323720
PubMed Link: 20346437
Variant Present in the following documents:
  • Main text
View BVdb publication page