rs4509693
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4509693(C;C) |
Make rs4509693(C;T) |
Make rs4509693(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 100741814 |
Gene | PAX2 |
is a | snp |
is | mentioned by |
dbSNP | rs4509693 |
dbSNP (classic) | rs4509693 |
ClinGen | rs4509693 |
ebi | rs4509693 |
HLI | rs4509693 |
Exac | rs4509693 |
Gnomad | rs4509693 |
Varsome | rs4509693 |
LitVar | rs4509693 |
Map | rs4509693 |
PheGenI | rs4509693 |
Biobank | rs4509693 |
1000 genomes | rs4509693 |
hgdp | rs4509693 |
ensembl | rs4509693 |
geneview | rs4509693 |
scholar | rs4509693 |
rs4509693 | |
pharmgkb | rs4509693 |
gwascentral | rs4509693 |
openSNP | rs4509693 |
23andMe | rs4509693 |
SNPshot | rs4509693 |
SNPdbe | rs4509693 |
MSV3d | rs4509693 |
GWAS Ctlg | rs4509693 |
GMAF | 0.1708 |
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 | 0.000006 |
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 | 0.000006 |
Odds Ratio | None None |