GALC c.196-1692G>T

Variant ID: 14-88456559-C-A

NM_000153.3(GALC):c.196-1692G>T

This variant was identified in 2 publications

View GRCh38 version.




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: rs8014798
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record.

Thrombosis And Haemostasis
Karnes, Jason H JH; Cronin, Robert M RM; Rollin, Jerome J; Teumer, Alexander A; Pouplard, Claire C; Shaffer, Christian M CM; Blanquicett, Carmelo C; Bowton, Erica A EA; Cowan, James D JD; Mosley, Jonathan D JD; Van Driest, Sara L SL; Weeke, Peter E PE; Wells, Quinn S QS; Bakchoul, Tamam T; Denny, Joshua C JC; Greinacher, Andreas A; Gruel, Yves Y; Roden, Dan M DM
Publication Date: 2015-04

Variant appearance in text: rs8014798
PubMed Link: 25503805
Variant Present in the following documents:
  • Main text
View BVdb publication page