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DMGDH c.2386-1734A>C
Variant ID: 5-78295854-T-G
NM_013391.3(
DMGDH
):c.2386-1734A>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:
Mendelian randomization: a novel approach for the prediction of adverse drug events and drug repurposing opportunities.
International Journal Of Epidemiology
Walker, Venexia M VM; Davey Smith, George G; Davies, Neil M NM; Martin, Richard M RM
Publication Date: 2017-12-01
Variant appearance in text: rs28326
PubMed Link:
29040597
Variant Present in the following documents:
Main text
dyx207.pdf
View BVdb publication page