rs17443013
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17443013(C;C) |
Make rs17443013(C;T) |
Make rs17443013(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 41133527 |
Gene | APBB2 |
is a | snp |
is | mentioned by |
dbSNP | rs17443013 |
dbSNP (classic) | rs17443013 |
ClinGen | rs17443013 |
ebi | rs17443013 |
HLI | rs17443013 |
Exac | rs17443013 |
Gnomad | rs17443013 |
Varsome | rs17443013 |
LitVar | rs17443013 |
Map | rs17443013 |
PheGenI | rs17443013 |
Biobank | rs17443013 |
1000 genomes | rs17443013 |
hgdp | rs17443013 |
ensembl | rs17443013 |
geneview | rs17443013 |
scholar | rs17443013 |
rs17443013 | |
pharmgkb | rs17443013 |
gwascentral | rs17443013 |
openSNP | rs17443013 |
23andMe | rs17443013 |
SNPshot | rs17443013 |
SNPdbe | rs17443013 |
MSV3d | rs17443013 |
GWAS Ctlg | rs17443013 |
GMAF | 0.494 |
Max Magnitude | 0 |
[PMID 18852029] Analysis of APBB2 gene polymorphisms in sporadic Alzheimer's disease.
[PMID 23384821] APBB2 genetic polymorphisms are associated with severe cognitive impairment in centenarians.