PTPN22 c.1852C>G ;(p.P618A)

Variant ID: 1-114377574-G-C

NM_015967.5(PTPN22):c.1852C>G;(p.P618A)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Genetic Basis of Common Human Disease: Insight into the Role of Missense SNPs from Genome-Wide Association Studies.

Journal Of Molecular Biology
Pal, Lipika R LR; Moult, John J
Publication Date: 2015-07-03

Variant appearance in text: PTPN22: P618A
PubMed Link: 25937569
Variant Present in the following documents:
  • Main text
View BVdb publication page



The autoimmunity risk variant LYP-W620 cooperates with CSK in the regulation of TCR signaling.

Plos One
de la Puerta, María Luisa ML; Trinidad, Antonio G AG; Rodríguez, María del Carmen Mdel C; de Pereda, José María JM; Sánchez Crespo, Mariano M; Bayón, Yolanda Y; Alonso, Andrés A
Publication Date: 2013

Variant appearance in text: PTPN22: P618A
PubMed Link: 23359562
Variant Present in the following documents:
  • Main text
  • pone.0054569.pdf
View BVdb publication page