rs78117248
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
(A;G) | 2 | risk factor for Alzheimer disease (odds ratio ~2x) |
Make rs78117248(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 1052854 |
Gene | ABCA7 |
is a | snp |
is | mentioned by |
dbSNP | rs78117248 |
dbSNP (classic) | rs78117248 |
ClinGen | rs78117248 |
ebi | rs78117248 |
HLI | rs78117248 |
Exac | rs78117248 |
Gnomad | rs78117248 |
Varsome | rs78117248 |
LitVar | rs78117248 |
Map | rs78117248 |
PheGenI | rs78117248 |
Biobank | rs78117248 |
1000 genomes | rs78117248 |
hgdp | rs78117248 |
ensembl | rs78117248 |
geneview | rs78117248 |
scholar | rs78117248 |
rs78117248 | |
pharmgkb | rs78117248 |
gwascentral | rs78117248 |
openSNP | rs78117248 |
23andMe | rs78117248 |
SNPshot | rs78117248 |
SNPdbe | rs78117248 |
MSV3d | rs78117248 |
GWAS Ctlg | rs78117248 |
Max Magnitude | 2 |
Sequencing of the ABCA7 gene in a Belgian cohort of 700+ patients with Alzheimer's disease led to the association of the rare rs78117248(G) allele with increased risk (odds ratio 2.07, CI: 1.31-3.27, p=0.0016).[PMID 26141617]