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APOE c.172G>A ;(p.V58M)
Variant ID: 19-45411145-G-A
NM_000041.2(
APOE
):c.172G>A;(p.V58M)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
APOE and COMT polymorphisms are complementary biomarkers of status, stability, and transitions in normal aging and early mild cognitive impairment.
Frontiers In Aging Neuroscience
Dixon, Roger A RA; DeCarlo, Correne A CA; MacDonald, Stuart W S SW; Vergote, David D; Jhamandas, Jack J; Westaway, David D
Publication Date: 2014
Variant appearance in text: APOE: Val58Met
PubMed Link:
25249975
Variant Present in the following documents:
fnagi-06-00236.pdf
View BVdb publication page
Hypothesis-driven candidate genes for schizophrenia compared to genome-wide association results.
Psychological Medicine
Collins, A L AL; Kim, Y Y; Sklar, P P; , ; O'Donovan, M C MC; Sullivan, P F PF
Publication Date: 2012-03
Variant appearance in text: APOE: val58met
PubMed Link:
21854684
Variant Present in the following documents:
Main text
View BVdb publication page