Bibliome.ai browser hg19
Search
About
Stats
FAQ
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.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
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