rs10792830
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10792830(A;A) |
Make rs10792830(A;G) |
Make rs10792830(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 86127766 |
is a | snp |
is | mentioned by |
dbSNP | rs10792830 |
dbSNP (classic) | rs10792830 |
ClinGen | rs10792830 |
ebi | rs10792830 |
HLI | rs10792830 |
Exac | rs10792830 |
Gnomad | rs10792830 |
Varsome | rs10792830 |
LitVar | rs10792830 |
Map | rs10792830 |
PheGenI | rs10792830 |
Biobank | rs10792830 |
1000 genomes | rs10792830 |
hgdp | rs10792830 |
ensembl | rs10792830 |
geneview | rs10792830 |
scholar | rs10792830 |
rs10792830 | |
pharmgkb | rs10792830 |
gwascentral | rs10792830 |
openSNP | rs10792830 |
23andMe | rs10792830 |
SNPshot | rs10792830 |
SNPdbe | rs10792830 |
MSV3d | rs10792830 |
GWAS Ctlg | rs10792830 |
GMAF | 0.4706 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22005930![]() |
Trait | |
Title | Genome-wide association study of Alzheimer's disease with psychotic symptoms. |
Risk Allele | |
P-val | 0.000006 |
Odds Ratio | 1.2500 None |