RGL3 c.637+431C>T

Variant ID: 19-11526182-G-A

NM_001035223.2(RGL3):c.637+431C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-Wide Association Studies of Hypertension and Several Other Cardiovascular Diseases.

Pulse (Basel, Switzerland)
Wang, Yan Y; Wang, Ji-Guang JG
Publication Date: 2019-04

Variant appearance in text: rs77279095
PubMed Link: 31049317
Variant Present in the following documents:
  • Main text
View BVdb publication page