rs10207628
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10207628(C;C) |
Make rs10207628(C;G) |
Make rs10207628(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 127094445 |
Gene | BIN1 |
is a | snp |
is | mentioned by |
dbSNP | rs10207628 |
dbSNP (classic) | rs10207628 |
ClinGen | rs10207628 |
ebi | rs10207628 |
HLI | rs10207628 |
Exac | rs10207628 |
Gnomad | rs10207628 |
Varsome | rs10207628 |
LitVar | rs10207628 |
Map | rs10207628 |
PheGenI | rs10207628 |
Biobank | rs10207628 |
1000 genomes | rs10207628 |
hgdp | rs10207628 |
ensembl | rs10207628 |
geneview | rs10207628 |
scholar | rs10207628 |
rs10207628 | |
pharmgkb | rs10207628 |
gwascentral | rs10207628 |
openSNP | rs10207628 |
23andMe | rs10207628 |
SNPshot | rs10207628 |
SNPdbe | rs10207628 |
MSV3d | rs10207628 |
GWAS Ctlg | rs10207628 |
GMAF | 0.1818 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 0.000001 |
Odds Ratio | 1.4100 None |