rs7539409
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common on affy axiom data |
Make rs7539409(A;G) |
Make rs7539409(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 83789052 |
Gene | LINC01725 |
is a | snp |
is | mentioned by |
dbSNP | rs7539409 |
dbSNP (classic) | rs7539409 |
ClinGen | rs7539409 |
ebi | rs7539409 |
HLI | rs7539409 |
Exac | rs7539409 |
Gnomad | rs7539409 |
Varsome | rs7539409 |
LitVar | rs7539409 |
Map | rs7539409 |
PheGenI | rs7539409 |
Biobank | rs7539409 |
1000 genomes | rs7539409 |
hgdp | rs7539409 |
ensembl | rs7539409 |
geneview | rs7539409 |
scholar | rs7539409 |
rs7539409 | |
pharmgkb | rs7539409 |
gwascentral | rs7539409 |
openSNP | rs7539409 |
23andMe | rs7539409 |
SNPshot | rs7539409 |
SNPdbe | rs7539409 |
MSV3d | rs7539409 |
GWAS Ctlg | rs7539409 |
GMAF | 0.08173 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 0.000001 |
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 | 0.000001 |
Odds Ratio | None None |