PTPN22 c.828+1496T>G

Variant ID: 1-114393153-A-C

NM_015967.5(PTPN22):c.828+1496T>G

This variant was identified in 6 publications

View GRCh38 version.




Publications:


The haplotypes of various TNF related genes associated with scleritis in Chinese Han.

Human Genomics
Gao, Yingnan Y; Du, Liping L; Li, Fuzhen F; Ding, Jiadong J; Li, Geng G; Cao, Qingfeng Q; Li, Na N; Su, Guannan G; Kijlstra, Aize A; Yang, Peizeng P
Publication Date: 2020-12-07

Variant appearance in text: rs1217406
PubMed Link: 33287909
Variant Present in the following documents:
  • Main text
  • 40246_2020_Article_296.pdf
View BVdb publication page



Multiomics dissection of molecular regulatory mechanisms underlying autoimmune-associated noncoding SNPs.

Jci Insight
Chen, Xiao-Feng XF; Guo, Ming-Rui MR; Duan, Yuan-Yuan YY; Jiang, Feng F; Wu, Hao H; Dong, Shan-Shan SS; Zhou, Xiao-Rong XR; Thynn, Hlaing Nwe HN; Liu, Cong-Cong CC; Zhang, Lin L; Guo, Yan Y; Yang, Tie-Lin TL
Publication Date: 2020-09-03

Variant appearance in text: rs1217406
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Identification of susceptibility SNPs in CTLA-4 and PTPN22 for scleritis in Han Chinese.

Clinical And Experimental Immunology
Li, F F; Ma, X X; Du, L L; Shi, L L; Cao, Q Q; Li, N N; Pang, T T; Liu, Y Y; Kijlstra, A A; Yang, P P
Publication Date: 2019-08

Variant appearance in text: rs1217406
PubMed Link: 30921471
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association of PTPN22 polymorphsims and ankylosing spondylitis susceptibility.

International Journal Of Clinical And Experimental Pathology
Meng, Qingxi Q; Zhang, Xiaojun X; Liu, Xin X; Wang, Weiguo W; Yu, Peng P; Shan, Qunqun Q; Mao, Zhaohu Z; Zhao, Tingbao T
Publication Date: 2015

Variant appearance in text: rs1217406
PubMed Link: 25755798
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene- or region-based association study via kernel principal component analysis.

Bmc Genetics
Gao, Qingsong Q; He, Yungang Y; Yuan, Zhongshang Z; Zhao, Jinghua J; Zhang, Bingbing B; Xue, Fuzhong F
Publication Date: 2011-08-26

Variant appearance in text: rs1217406
PubMed Link: 21871061
Variant Present in the following documents:
  • Main text
  • 1471-2156-12-75.pdf
View BVdb publication page



PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.

American Journal Of Human Genetics
Carlton, Victoria E H VE; Hu, Xiaolan X; Chokkalingam, Anand P AP; Schrodi, Steven J SJ; Brandon, Rhonda R; Alexander, Heather C HC; Chang, Monica M; Catanese, Joseph J JJ; Leong, Diane U DU; Ardlie, Kristin G KG; Kastner, Daniel L DL; Seldin, Michael F MF; Criswell, Lindsey A LA; Gregersen, Peter K PK; Beasley, Ellen E; Thomson, Glenys G; Amos, Christopher I CI; Begovich, Ann B AB
Publication Date: 2005-10

Variant appearance in text: rs1217406
PubMed Link: 16175503
Variant Present in the following documents:
  • Main text
View BVdb publication page