TSHR c.171-4085T>C

Variant ID: 14-81524407-T-C

NM_000369.2(TSHR):c.171-4085T>C

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Association between TSHR gene polymorphism and the risk of Graves' disease: a meta-analysis.

Journal Of Biomedical Research
Qian, Wei W; Xu, Kuanfeng K; Jia, Wenting W; Lan, Ling L; Zheng, Xuqin X; Yang, Xueyang X; Cui, Dai D
Publication Date: 2016-11

Variant appearance in text: rs2268474
PubMed Link: 27231040
Variant Present in the following documents:
  • Main text
  • jbr-30-06-466.pdf
View BVdb publication page



The genetic basis of graves' disease.

Current Genomics
Płoski, Rafał R; Szymański, Konrad K; Bednarczuk, Tomasz T
Publication Date: 2011-12

Variant appearance in text: rs2268474
PubMed Link: 22654555
Variant Present in the following documents:
  • Main text
  • CG-12-542.pdf
View BVdb publication page



Thyroid stimulating hormone receptor (TSHR) intron 1 variants are major risk factors for Graves' disease in three European Caucasian cohorts.

Plos One
Płoski, Rafał R; Brand, Oliver J OJ; Jurecka-Lubieniecka, Beata B; Franaszczyk, Maria M; Kula, Dorota D; Krajewski, Paweł P; Karamat, Muhammad A MA; Simmonds, Matthew J MJ; Franklyn, Jayne A JA; Gough, Stephen C L SC; Jarząb, Barbara B; Bednarczuk, Tomasz T
Publication Date: 2010-11-25

Variant appearance in text: rs2268474
PubMed Link: 21124799
Variant Present in the following documents:
  • Main text
  • pone.0015512.pdf
View BVdb publication page