PSEN1 c.*3632G>A

Variant ID: 14-73689629-G-A

NM_000021.3(PSEN1):c.*3632G>A

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease.

Scientific Reports
Elsheikh, Samar S M SSM; Chimusa, Emile R ER; Mulder, Nicola J NJ; Crimi, Alessandro A
Publication Date: 2020-01-29

Variant appearance in text: rs362393
PubMed Link: 31996736
Variant Present in the following documents:
  • Main text
  • 41598_2020_Article_58291.pdf
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs362393
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page