HERC2 c.187+669C>T

Variant ID: 15-28543879-G-A

NM_004667.5(HERC2):c.187+669C>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: rs8023410
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page



Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes.

Human Molecular Genetics
Aponte, Jennifer L JL; Chiano, Mathias N MN; Yerges-Armstrong, Laura M LM; Hinds, David A DA; Tian, Chao C; Gupta, Akanksha A; Guo, Cong C; Fraser, Dana J DJ; Freudenberg, Johannes M JM; Rajpal, Deepak K DK; Ehm, Margaret G MG; Waterworth, Dawn M DM
Publication Date: 2018-08-01

Variant appearance in text: rs8023410
PubMed Link: 29771307
Variant Present in the following documents:
  • Main text
  • ddy184.pdf
View BVdb publication page