Bibliome.ai browser hg19
Search
About
Stats
FAQ
INSL6 c.289+3847G>T
Variant ID: 9-5181467-C-A
NM_007179.2(
INSL6
):c.289+3847G>T
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: rs7047795
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page
Convergent mechanisms of somatic mutations in polycythemia vera.
Discovery Medicine
Wang, Kai K; Swierczek, Sabina S; Hickman, Kimberly K; Hakonarson, Hakon H; Prchal, Josef T JT
Publication Date: 2011-07
Variant appearance in text: rs7047795
PubMed Link:
21794206
Variant Present in the following documents:
Main text
View BVdb publication page