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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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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