FXR2 c.661-1453G>A

Variant ID: 17-7500765-C-T

NM_004860.3(FXR2):c.661-1453G>A

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:

The Potential Effect of Aberrant Testosterone Levels on Common Diseases: A Mendelian Randomization Study.

Genes
Syed, Ali Alamdar Shah AAS; He, Lin L; Shi, Yongyong Y
Publication Date: 2020-06-29

Variant appearance in text: rs12936934
PubMed Link: 32610558
Variant Present in the following documents:
  • Main text
  • genes-11-00721.pdf
View BVdb publication page