ABCG1 c.1216A>T ;(p.R406W)

Variant ID: 21-43708414-A-T

NM_016818.2(ABCG1):c.1216A>T;(p.R406W)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry.

Jama Network Open
Patel, Devanshi D; Mez, Jesse J; Vardarajan, Badri N BN; Staley, Lyndsay L; Chung, Jaeyoon J; Zhang, Xiaoling X; Farrell, John J JJ; Rynkiewicz, Michael J MJ; Cannon-Albright, Lisa A LA; Teerlink, Craig C CC; Stevens, Jeffery J; Corcoran, Christopher C; Gonzalez Murcia, Josue D JD; Lopez, Oscar L OL; Mayeux, Richard R; Haines, Jonathan L JL; Pericak-Vance, Margaret A MA; Schellenberg, Gerard G; Kauwe, John S K JSK; Lunetta, Kathryn L KL; Farrer, Lindsay A LA; ,
Publication Date: 2019-03-01

Variant appearance in text: ABCG1: R406W
PubMed Link: 30924900
Variant Present in the following documents:
  • jamanetwopen-2-e191350-s001.pdf
View BVdb publication page