CRHR1 c.327+3699C>T

Variant ID: 17-43902505-C-T

NM_004382.4(CRHR1):c.327+3699C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer's disease, providing new insights into its disease mechanisms.

Scientific Reports
Wang, Zhen Z; Zhang, Quanwei Q; Lin, Jhih-Rong JR; Jabalameli, M Reza MR; Mitra, Joydeep J; Nguyen, Nha N; Zhang, Zhengdong D ZD
Publication Date: 2021-10-15

Variant appearance in text: rs4341787
PubMed Link: 34654853
Variant Present in the following documents:
  • Main text
  • 41598_2021_Article_99352.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: rs4341787
PubMed Link: 32879140
Variant Present in the following documents:
  • jciinsight-5-136477-s105.xlsx, sheet 5
View BVdb publication page