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APP c.57+9860G>C
Variant ID: 21-27533022-C-G
NM_000484.3(
APP
):c.57+9860G>C
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:
Implication of the APP Gene in Intellectual Abilities.
Journal Of Alzheimer'S Disease : Jad
Myrum, Craig C; Nikolaienko, Oleksii O; Bramham, Clive R CR; Haavik, Jan J; Zayats, Tetyana T
Publication Date: 2017
Variant appearance in text: rs465235
PubMed Link:
28671113
Variant Present in the following documents:
Main text
jad-59-jad170049.pdf
View BVdb publication page
An efficient method for multi-locus molecular haplotyping.
Nucleic Acids Research
Konfortov, Bernard A BA; Bankier, Alan T AT; Dear, Paul H PH
Publication Date: 2007
Variant appearance in text: rs465235
PubMed Link:
17158153
Variant Present in the following documents:
gkl742.pdf
View BVdb publication page