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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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