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RBFOX1 c.676+9888A>G
Variant ID: 16-7667228-A-G
NM_018723.3(
RBFOX1
):c.676+9888A>G
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis.
Frontiers In Psychiatry
Yin, Bian B; Wang, Xinpei X; Huang, Tao T; Jia, Jinzhu J
Publication Date: 2022
Variant appearance in text: rs3785235
PubMed Link:
35898629
Variant Present in the following documents:
Main text
fpsyt-13-910432.pdf
View BVdb publication page