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ACAD10 c.2817+691A>G
Variant ID: 12-112187840-A-G
NM_025247.5(
ACAD10
):c.2817+691A>G
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: rs11608345
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page
Mendelian randomization: a novel approach for the prediction of adverse drug events and drug repurposing opportunities.
International Journal Of Epidemiology
Walker, Venexia M VM; Davey Smith, George G; Davies, Neil M NM; Martin, Richard M RM
Publication Date: 2017-12-01
Variant appearance in text: rs11608345
PubMed Link:
29040597
Variant Present in the following documents:
Main text
dyx207.pdf
View BVdb publication page