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BRD7 c.591+857G>A
Variant ID: 16-50383077-C-T
NM_013263.4(
BRD7
):c.591+857G>A
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:
Identification of multiple novel susceptibility genes associated with autoimmune thyroid disease.
Frontiers In Immunology
Liu, Xueying X; Miao, Yahu Y; Liu, Chao C; Lu, Wan W; Feng, Qing Q; Zhang, Qiu Q
Publication Date: 2023
Variant appearance in text: rs9934775
PubMed Link:
37197658
Variant Present in the following documents:
Main text
View BVdb publication page
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: rs9934775
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page