PTPN22 c.915+37T>C

Variant ID: 1-114391125-A-G

NM_015967.5(PTPN22):c.915+37T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


MAGPEL: an autoMated pipeline for inferring vAriant-driven Gene PanEls from the full-length biomedical literature.

Scientific Reports
Saberian, Nafiseh N; Shafi, Adib A; Peyvandipour, Azam A; Draghici, Sorin S
Publication Date: 2020-07-23

Variant appearance in text: rs3827734
PubMed Link: 32703994
Variant Present in the following documents:
  • 41598_2020_68649_MOESM2_ESM.xlsx, sheet 2
View BVdb publication page



Extra-binomial variation approach for analysis of pooled DNA sequencing data.

Bioinformatics (Oxford, England)
Yang, Xin X; Todd, John A JA; Clayton, David D; Wallace, Chris C
Publication Date: 2012-11-15

Variant appearance in text: rs3827734
PubMed Link: 22976083
Variant Present in the following documents:
  • Main text
  • bts553.pdf
View BVdb publication page



Genetic risk factors for rheumatoid arthritis differ in Caucasian and Korean populations.

Arthritis And Rheumatism
Lee, Hye-Soon HS; Korman, Benjamin D BD; Le, Julie M JM; Kastner, Daniel L DL; Remmers, Elaine F EF; Gregersen, Peter K PK; Bae, Sang-Cheol SC
Publication Date: 2009-02

Variant appearance in text: rs3827734
PubMed Link: 19180477
Variant Present in the following documents:
  • Main text
View BVdb publication page