TG c.7862+5713C>T

Variant ID: 8-134134673-C-T

NM_003235.4(TG):c.7862+5713C>T

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Molecular Mechanisms in Autoimmune Thyroid Disease.

Cells
Vargas-Uricoechea, Hernando H
Publication Date: 2023-03-16

Variant appearance in text: rs2958692
PubMed Link: 36980259
Variant Present in the following documents:
  • Main text
  • cells-12-00918.pdf
View BVdb publication page



Genetics, Epigenetics, Cellular Immunology, and Gut Microbiota: Emerging Links With Graves' Disease.

Frontiers In Cell And Developmental Biology
Zhou, Fangyu F; Wang, Xin X; Wang, Lingjun L; Sun, Xin X; Tan, Guiqin G; Wei, Wenwen W; Zheng, Guangbing G; Ma, Xiaomin X; Tian, Dan D; Yu, Hongsong H
Publication Date: 2021

Variant appearance in text: rs2958692
PubMed Link: 35059400
Variant Present in the following documents:
  • Main text
  • fcell-09-794912.pdf
View BVdb publication page



Fine mapping of thyroglobulin gene identifies two independent risk loci for Graves' disease in Chinese Han population.

Annals Of Translational Medicine
Xuan, Miao M; Zhao, Shuang-Xia SX; Yan, Chen-Yan CY; Yang, Jun J; Li, Ying Y; Song, Li-Ge LG; Song, Huai-Dong HD; Zhang, Xiu-Zhen XZ
Publication Date: 2019-09

Variant appearance in text: rs2958692
PubMed Link: 31700870
Variant Present in the following documents:
  • Main text
View BVdb publication page