rs9390537
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9390537(C;C) |
Make rs9390537(C;T) |
Make rs9390537(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 148102235 |
is a | snp |
is | mentioned by |
dbSNP | rs9390537 |
dbSNP (classic) | rs9390537 |
ClinGen | rs9390537 |
ebi | rs9390537 |
HLI | rs9390537 |
Exac | rs9390537 |
Gnomad | rs9390537 |
Varsome | rs9390537 |
LitVar | rs9390537 |
Map | rs9390537 |
PheGenI | rs9390537 |
Biobank | rs9390537 |
1000 genomes | rs9390537 |
hgdp | rs9390537 |
ensembl | rs9390537 |
geneview | rs9390537 |
scholar | rs9390537 |
rs9390537 | |
pharmgkb | rs9390537 |
gwascentral | rs9390537 |
openSNP | rs9390537 |
23andMe | rs9390537 |
SNPshot | rs9390537 |
SNPdbe | rs9390537 |
MSV3d | rs9390537 |
GWAS Ctlg | rs9390537 |
GMAF | 0.3774 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 19749422] |
Trait | Alzheimer's Disease |
Title | Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | NR NR |
GWAS snp | |
---|---|
PMID | [PMID 20061627] |
Trait | Alzheimer's disease |
Title | Genome-wide scan of copy number variation in late-onset Alzheimer's disease. |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | None None |