APOE c.394C>A ;(p.R132S)

Variant ID: 19-45411947-C-A

NM_000041.2(APOE):c.394C>A;(p.R132S)

This variant was identified in 4 publications

View GRCh38 version.




Publications:


Methodological quality assessment of genetic studies on brain arteriovenous malformation related hemorrhage: A cross-sectional study.

Frontiers In Genetics
Jiang, Junhao J; Qin, Zhuo Z; Yan, Junxia J; Liu, Junyu J
Publication Date: 2023

Variant appearance in text: rs11542041
PubMed Link: 37065486
Variant Present in the following documents:
  • Main text
  • fgene-14-1123898.pdf
View BVdb publication page



Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.

Journal Of Lipid Research
Zhou, Yitian Y; Mägi, Reedik R; Milani, Lili L; Lauschke, Volker M VM
Publication Date: 2018-10

Variant appearance in text: rs11542041
PubMed Link: 30076208
Variant Present in the following documents:
  • 10.1194_P086710_jlr.P086710-4.xlsx, sheet 3
View BVdb publication page



In silico analyses of deleterious missense SNPs of human apolipoprotein E3.

Scientific Reports
Pires, Allan S AS; Porto, William F WF; Franco, Octavio L OL; Alencar, Sérgio A SA
Publication Date: 2017-05-30

Variant appearance in text: APOE: Arg132Ser; rs11542041
PubMed Link: 28559539
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_1737.pdf
View BVdb publication page



Screening and Evaluation of Deleterious SNPs in APOE Gene of Alzheimer's Disease.

Neurology Research International
Masoodi, Tariq Ahmad TA; Al Shammari, Sulaiman A SA; Al-Muammar, May N MN; Alhamdan, Adel A AA
Publication Date: 2012

Variant appearance in text: APOE: R132S; rs11542041
PubMed Link: 22530123
Variant Present in the following documents:
  • Main text
  • NRI2012-480609.pdf
View BVdb publication page