PTPN22 c.916-783C>A

Variant ID: 1-114382025-G-T

NM_015967.5(PTPN22):c.916-783C>A

This variant was identified in 4 publications

View GRCh38 version.




Publications:


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: rs974404
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



SNM1B/Apollo in the DNA damage response and telomere maintenance.

Oncotarget
Schmiester, Maren M; Demuth, Ilja I
Publication Date: 2017-07-18

Variant appearance in text: rs974404
PubMed Link: 28430596
Variant Present in the following documents:
  • Main text
  • oncotarget-08-48398.pdf
View BVdb publication page



Telomere structure and maintenance gene variants and risk of five cancer types.

International Journal Of Cancer
Karami, Sara S; Han, Younghun Y; Pande, Mala M; Cheng, Iona I; Rudd, James J; Pierce, Brandon L BL; Nutter, Ellen L EL; Schumacher, Fredrick R FR; Kote-Jarai, Zsofia Z; Lindstrom, Sara S; Witte, John S JS; Fang, Shenying S; Han, Jiali J; Kraft, Peter P; Hunter, David J DJ; Song, Fengju F; Hung, Rayjean J RJ; McKay, James J; Gruber, Stephen B SB; Chanock, Stephen J SJ; Risch, Angela A; Shen, Hongbing H; Haiman, Christopher A CA; Boardman, Lisa L; Ulrich, Cornelia M CM; Casey, Graham G; Peters, Ulrike U; Amin Al Olama, Ali A; Berchuck, Andrew A; Berndt, Sonja I SI; Bezieau, Stephane S; Brennan, Paul P; Brenner, Hermann H; Brinton, Louise L; Caporaso, Neil N; Chan, Andrew T AT; Chang-Claude, Jenny J; Christiani, David C DC; Cunningham, Julie M JM; Easton, Douglas D; Eeles, Rosalind A RA; Eisen, Timothy T; Gala, Manish M; Gallinger, Steven J SJ; Gayther, Simon A SA; Goode, Ellen L EL; Grönberg, Henrik H; Henderson, Brian E BE; Houlston, Richard R; Joshi, Amit D AD; Küry, Sébastien S; Landi, Mari T MT; Le Marchand, Loic L; Muir, Kenneth K; Newcomb, Polly A PA; Permuth-Wey, Jenny J; Pharoah, Paul P; Phelan, Catherine C; Potter, John D JD; Ramus, Susan J SJ; Risch, Harvey H; Schildkraut, Joellen J; Slattery, Martha L ML; Song, Honglin H; Wentzensen, Nicolas N; White, Emily E; Wiklund, Fredrik F; Zanke, Brent W BW; Sellers, Thomas A TA; Zheng, Wei W; Chatterjee, Nilanjan N; Amos, Christopher I CI; Doherty, Jennifer A JA; ,
Publication Date: 2016-12-15

Variant appearance in text: rs974404
PubMed Link: 27459707
Variant Present in the following documents:
  • Main text
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: rs974404
PubMed Link: 16175503
Variant Present in the following documents:
  • Main text
View BVdb publication page