rs17189298
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17189298(A;A) |
Make rs17189298(A;G) |
Make rs17189298(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 119087741 |
is a | snp |
is | mentioned by |
dbSNP | rs17189298 |
dbSNP (classic) | rs17189298 |
ClinGen | rs17189298 |
ebi | rs17189298 |
HLI | rs17189298 |
Exac | rs17189298 |
Gnomad | rs17189298 |
Varsome | rs17189298 |
LitVar | rs17189298 |
Map | rs17189298 |
PheGenI | rs17189298 |
Biobank | rs17189298 |
1000 genomes | rs17189298 |
hgdp | rs17189298 |
ensembl | rs17189298 |
geneview | rs17189298 |
scholar | rs17189298 |
rs17189298 | |
pharmgkb | rs17189298 |
gwascentral | rs17189298 |
openSNP | rs17189298 |
23andMe | rs17189298 |
SNPshot | rs17189298 |
SNPdbe | rs17189298 |
MSV3d | rs17189298 |
GWAS Ctlg | rs17189298 |
GMAF | 0.3489 |
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 | A |
P-val | 3E-7 |
Odds Ratio | None None |