PDCD1 c.628-110A>G

Variant ID: 2-242793559-T-C

NM_005018.2(PDCD1):c.628-110A>G

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Association between the side effect induced by COVID-19 vaccines and the immune regulatory gene polymorphism.

Frontiers In Immunology
Chen, Ding-Ping DP; Wen, Ying-Hao YH; Lin, Wei-Tzu WT; Hsu, Fang-Ping FP
Publication Date: 2022

Variant appearance in text: rs6705653
PubMed Link: 36389676
Variant Present in the following documents:
  • Main text
  • fimmu-13-941497.pdf
View BVdb publication page



Investigation of the association between the genetic polymorphisms of the co-stimulatory system and systemic lupus erythematosus.

Frontiers In Immunology
Chen, Ding-Ping DP; Lin, Wei-Tzu WT; Yu, Kuang-Hui KH
Publication Date: 2022

Variant appearance in text: rs6705653
PubMed Link: 36189300
Variant Present in the following documents:
  • Main text
  • fimmu-13-946456.pdf
View BVdb publication page



Single-Nucleotide Polymorphisms Within Non-HLA Regions Are Associated With Engraftment Effectiveness for Patients With Unrelated Cord Blood Transplantation.

Frontiers In Immunology
Chen, Ding-Ping DP; Jaing, Tang-Her TH; Hour, Ai-Ling AL; Lin, Wei-Tzu WT; Hsu, Fang-Ping FP
Publication Date: 2022

Variant appearance in text: rs6705653
PubMed Link: 35769457
Variant Present in the following documents:
  • Main text
  • fimmu-13-888204.pdf
View BVdb publication page



The Association Between Single-Nucleotide Polymorphisms of Co-Stimulatory Genes Within Non-HLA Region and the Prognosis of Leukemia Patients With Hematopoietic Stem Cell Transplantation.

Frontiers In Immunology
Chen, Ding-Ping DP; Chang, Su-Wei SW; Wang, Po-Nan PN; Lin, Wei-Tzu WT; Hsu, Fang-Ping FP; Wang, Wei-Ting WT; Tseng, Ching-Ping CP
Publication Date: 2021

Variant appearance in text: rs6705653
PubMed Link: 34671352
Variant Present in the following documents:
  • Main text
  • fimmu-12-730507.pdf
View BVdb publication page



Association between PDCD1 gene polymorphisms and psoriasis susceptibility in the Chinese population.

International Journal Of Dermatology
Hua, Shengyuan S; Fan, Bin B; Mao, Weiwei W; Xu, Rong R; Wang, Yifei Y; Kuai, Le L; Ding, Xiaojie X; Li, Bin B; Chen, Jie J; Miao, Xiao X
Publication Date: 2021-11

Variant appearance in text: rs6705653
PubMed Link: 34057203
Variant Present in the following documents:
  • Main text
  • IJD-60-1411.pdf
View BVdb publication page



Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: PDCD1: 628-110A>G; rs6705653
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: PDCD1: 628-110A>G; rs6705653
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 2
  • CNR2-4-e1335-s003.xlsx, sheet 1
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: PDCD1: 628-110A>G; rs6705653
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort.

Genes And Immunity
Thorburn, C M CM; Prokunina-Olsson, L L; Sterba, K A KA; Lum, R F RF; Seldin, M F MF; Alarcon-Riquelme, M E ME; Criswell, L A LA
Publication Date: 2007-06

Variant appearance in text: rs6705653
PubMed Link: 17344889
Variant Present in the following documents:
  • Main text
View BVdb publication page