PGAP3 c.433-2668C>T

Variant ID: 17-37833600-G-A

NM_033419.3(PGAP3):c.433-2668C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Heritability Enrichment of Immunoglobulin G N-Glycosylation in Specific Tissues.

Frontiers In Immunology
Li, Xingang X; Wang, Hao H; Zhu, Yahong Y; Cao, Weijie W; Song, Manshu M; Wang, Youxin Y; Hou, Haifeng H; Lang, Minglin M; Guo, Xiuhua X; Tan, Xuerui X; Han, Jingdong J JJ; Wang, Wei W
Publication Date: 2021

Variant appearance in text: rs907089
PubMed Link: 34804021
Variant Present in the following documents:
  • Main text
  • fimmu-12-741705.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: rs907089
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer.

British Journal Of Cancer
Benusiglio, P R PR; Pharoah, P D PD; Smith, P L PL; Lesueur, F F; Conroy, D D; Luben, R N RN; Dew, G G; Jordan, C C; Dunning, A A; Easton, D F DF; Ponder, B A J BA
Publication Date: 2006-12-18

Variant appearance in text: rs907089
PubMed Link: 17117180
Variant Present in the following documents:
  • Main text
  • 95-6603473a.pdf
View BVdb publication page