rs115675626
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs115675626(A;A) |
Make rs115675626(A;G) |
Make rs115675626(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 6 |
Position | 32702056 |
is a | snp |
is | mentioned by |
dbSNP | rs115675626 |
dbSNP (classic) | rs115675626 |
ClinGen | rs115675626 |
ebi | rs115675626 |
HLI | rs115675626 |
Exac | rs115675626 |
Gnomad | rs115675626 |
Varsome | rs115675626 |
LitVar | rs115675626 |
Map | rs115675626 |
PheGenI | rs115675626 |
Biobank | rs115675626 |
1000 genomes | rs115675626 |
hgdp | rs115675626 |
ensembl | rs115675626 |
geneview | rs115675626 |
scholar | rs115675626 |
rs115675626 | |
pharmgkb | rs115675626 |
gwascentral | rs115675626 |
openSNP | rs115675626 |
23andMe | rs115675626 |
SNPshot | rs115675626 |
SNPdbe | rs115675626 |
MSV3d | rs115675626 |
GWAS Ctlg | rs115675626 |
Max Magnitude | 0 |
[PMID 28323831] Alzheimer's disease polygenic hazard score