POLG c.2426+281A>G

Variant ID: 15-89865692-T-C

NM_002693.2(POLG):c.2426+281A>G

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways.

Alzheimer'S & Dementia : The Journal Of The Alzheimer'S Association
Sherva, Richard R; Gross, Alden A; Mukherjee, Shubhabrata S; Koesterer, Ryan R; Amouyel, Philippe P; Bellenguez, Celine C; Dufouil, Carole C; Bennett, David A DA; Chibnik, Lori L; Cruchaga, Carlos C; Del-Aguila, Jorge J; Farrer, Lindsay A LA; Mayeux, Richard R; Munsie, Leanne L; Winslow, Ashley A; Newhouse, Stephen S; Saykin, Andrew J AJ; Kauwe, John S K JSK; , ; Crane, Paul K PK; Green, Robert C RC
Publication Date: 2020-08

Variant appearance in text: rs3176205
PubMed Link: 32573913
Variant Present in the following documents:
  • Main text
View BVdb publication page



Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs3176205
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
View BVdb publication page