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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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