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