TSHR c.170+46760G>C

Variant ID: 14-81468954-G-C

NM_000369.2(TSHR):c.170+46760G>C

This variant was identified in 2 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: rs4903964
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Correlation of TSHR and CTLA-4 Single Nucleotide Polymorphisms with Graves Disease.

International Journal Of Genomics
Sun, Weihua W; Zhang, Xiaomei X; Wu, Jing J; Zhao, Wendi W; Zhao, Shuangxia S; Li, Minglong M
Publication Date: 2019

Variant appearance in text: rs4903964
PubMed Link: 31565653
Variant Present in the following documents:
  • Main text
  • IJG2019-6982623.pdf
View BVdb publication page