rs10784496
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10784496(A;A) |
Make rs10784496(A;G) |
Make rs10784496(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 65767191 |
Gene | RPSAP52 |
is a | snp |
is | mentioned by |
dbSNP | rs10784496 |
dbSNP (classic) | rs10784496 |
ClinGen | rs10784496 |
ebi | rs10784496 |
HLI | rs10784496 |
Exac | rs10784496 |
Gnomad | rs10784496 |
Varsome | rs10784496 |
LitVar | rs10784496 |
Map | rs10784496 |
PheGenI | rs10784496 |
Biobank | rs10784496 |
1000 genomes | rs10784496 |
hgdp | rs10784496 |
ensembl | rs10784496 |
geneview | rs10784496 |
scholar | rs10784496 |
rs10784496 | |
pharmgkb | rs10784496 |
gwascentral | rs10784496 |
openSNP | rs10784496 |
23andMe | rs10784496 |
SNPshot | rs10784496 |
SNPdbe | rs10784496 |
MSV3d | rs10784496 |
GWAS Ctlg | rs10784496 |
GMAF | 0.3939 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20932310![]() |
Trait | |
Title | Genome-wide association reveals genetic effects on human Abeta42 and tau protein levels in cerebrospinal fluids: a case control study |
Risk Allele | G |
P-val | 3E-7 |
Odds Ratio | None None |