rs4746003
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4746003(C;C) |
Make rs4746003(C;T) |
Make rs4746003(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 69778536 |
Gene | RPL5P26 |
is a | snp |
is | mentioned by |
dbSNP | rs4746003 |
dbSNP (classic) | rs4746003 |
ClinGen | rs4746003 |
ebi | rs4746003 |
HLI | rs4746003 |
Exac | rs4746003 |
Gnomad | rs4746003 |
Varsome | rs4746003 |
LitVar | rs4746003 |
Map | rs4746003 |
PheGenI | rs4746003 |
Biobank | rs4746003 |
1000 genomes | rs4746003 |
hgdp | rs4746003 |
ensembl | rs4746003 |
geneview | rs4746003 |
scholar | rs4746003 |
rs4746003 | |
pharmgkb | rs4746003 |
gwascentral | rs4746003 |
openSNP | rs4746003 |
23andMe | rs4746003 |
SNPshot | rs4746003 |
SNPdbe | rs4746003 |
MSV3d | rs4746003 |
GWAS Ctlg | rs4746003 |
GMAF | 0.2475 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 1.3000 None |