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PLG c.668+348G>A
Variant ID: 6-161136294-G-A
NM_000301.3(
PLG
):c.668+348G>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:
A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.
International Journal Of Molecular Epidemiology And Genetics
Moore, Amy A; Enquobahrie, Daniel A DA; Sanchez, Sixto E SE; Ananth, Cande V CV; Pacora, Percy N PN; Williams, Michelle A MA
Publication Date: 2012
Variant appearance in text: rs9295131
PubMed Link:
23205182
Variant Present in the following documents:
Main text
View BVdb publication page