PDE11A c.1789-9234C>T

Variant ID: 2-178602134-G-A

NM_016953.3(PDE11A):c.1789-9234C>T

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:

Genetic ancestry plays a central role in population pharmacogenomics.

Communications Biology
Yang, Hsin-Chou HC; Chen, Chia-Wei CW; Lin, Yu-Ting YT; Chu, Shih-Kai SK
Publication Date: 2021-02-05

Variant appearance in text: rs79740438
PubMed Link: 33547344
Variant Present in the following documents:
  • 42003_2021_1681_MOESM2_ESM.pdf
View BVdb publication page