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ACSL6 c.49+5657C>G
Variant ID: 5-131341541-G-C
NM_001009185.2(
ACSL6
):c.49+5657C>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:
Prioritizing autoimmunity risk variants for functional analyses by fine-mapping mutations under natural selection.
Nature Communications
Pankratov, Vasili V; Yunusbaeva, Milyausha M; Ryakhovsky, Sergei S; Zarodniuk, Maksym M; , ; Yunusbayev, Bayazit B
Publication Date: 2022-11-18
Variant appearance in text: rs7714191
PubMed Link:
36400766
Variant Present in the following documents:
41467_2022_34461_MOESM1_ESM.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: rs7714191
PubMed Link:
32879140
Variant Present in the following documents:
jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page