PRNP c.-11+176G>C

Variant ID: 20-4667334-G-C

NM_000311.5(PRNP):c.-11+176G>C

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Prion protein gene mutation detection using long-read Nanopore sequencing.

Scientific Reports
Kroll, François F; Dimitriadis, Athanasios A; Campbell, Tracy T; Darwent, Lee L; Collinge, John J; Mead, Simon S; Vire, Emmanuelle E
Publication Date: 2022-05-18

Variant appearance in text: rs6052766
PubMed Link: 35585119
Variant Present in the following documents:
  • 41598_2022_12130_MOESM2_ESM.pdf
View BVdb publication page



Targeted neurogenesis pathway-based gene analysis identifies ADORA2A associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease.

Neurobiology Of Aging
Horgusluoglu-Moloch, Emrin E; Nho, Kwangsik K; Risacher, Shannon L SL; Kim, Sungeun S; Foroud, Tatiana T; Shaw, Leslie M LM; Trojanowski, John Q JQ; Aisen, Paul S PS; Petersen, Ronald C RC; Jack, Clifford R CR; Lovestone, Simon S; Simmons, Andrew A; Weiner, Michael W MW; Saykin, Andrew J AJ; ,
Publication Date: 2017-12

Variant appearance in text: rs6052766
PubMed Link: 28941407
Variant Present in the following documents:
  • Main text
View BVdb publication page