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.




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