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ACAD10 c.336+1456G>A
Variant ID: 12-112141570-G-A
NM_025247.5(
ACAD10
):c.336+1456G>A
This variant was identified in 5 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Single nucleotide variants in microRNA biosynthesis genes in Mexican individuals.
Frontiers In Genetics
Juárez-Luis, Jesús J; Canseco-Ocaña, Moisés M; Cid-Soto, Miguel Angel MA; Castro-Martínez, Xochitl H XH; Martínez-Hernández, Angélica A; Orozco, Lorena L; Hernández-Zavala, Araceli A; Córdova, Emilio J EJ
Publication Date: 2023
Variant appearance in text: rs847892
PubMed Link:
36968598
Variant Present in the following documents:
Main text
fgene-14-1022912.pdf
View BVdb publication page
Positive selection acts on regulatory genetic variants in populations of European ancestry that affect ALDH2 gene expression.
Scientific Reports
Schaschl, Helmut H; Göllner, Tobias T; Morris, David L DL
Publication Date: 2022-03-16
Variant appearance in text: rs847892
PubMed Link:
35296751
Variant Present in the following documents:
Main text
41598_2022_Article_8588.pdf
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: rs847892
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page
Integrating Multi-Omics Data to Identify Novel Disease Genes and Single-Neucleotide Polymorphisms.
Frontiers In Genetics
Zhao, Sheng S; Jiang, Huijie H; Liang, Zong-Hui ZH; Ju, Hong H
Publication Date: 2019
Variant appearance in text: rs847892
PubMed Link:
32038707
Variant Present in the following documents:
Main text
fgene-10-01336.pdf
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: rs847892
PubMed Link:
29040597
Variant Present in the following documents:
Main text
dyx207.pdf
View BVdb publication page