FBN1 c.4747+5G>C

Variant ID: 15-48760130-C-G

NM_000138.4(FBN1):c.4747+5G>C

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:

Prediction of Probable Major Depressive Disorder in the Taiwan Biobank: An Integrated Machine Learning and Genome-Wide Analysis Approach.

Journal Of Personalized Medicine
Lin, Eugene E; Kuo, Po-Hsiu PH; Lin, Wan-Yu WY; Liu, Yu-Li YL; Yang, Albert C AC; Tsai, Shih-Jen SJ
Publication Date: 2021-06-24

Variant appearance in text: rs193922209
PubMed Link: 34202750
Variant Present in the following documents:
  • Main text
  • jpm-11-00597.pdf
View BVdb publication page