rs118048115
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common genotype |
Make rs118048115(A;T) |
Make rs118048115(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 120519964 |
Gene | PLPP4 |
is a | snp |
is | mentioned by |
dbSNP | rs118048115 |
dbSNP (classic) | rs118048115 |
ClinGen | rs118048115 |
ebi | rs118048115 |
HLI | rs118048115 |
Exac | rs118048115 |
Gnomad | rs118048115 |
Varsome | rs118048115 |
LitVar | rs118048115 |
Map | rs118048115 |
PheGenI | rs118048115 |
Biobank | rs118048115 |
1000 genomes | rs118048115 |
hgdp | rs118048115 |
ensembl | rs118048115 |
geneview | rs118048115 |
scholar | rs118048115 |
rs118048115 | |
pharmgkb | rs118048115 |
gwascentral | rs118048115 |
openSNP | rs118048115 |
23andMe | rs118048115 |
SNPshot | rs118048115 |
SNPdbe | rs118048115 |
MSV3d | rs118048115 |
GWAS Ctlg | rs118048115 |
GMAF | 0.006887 |
Max Magnitude | 0 |
GWAS snp | |
---|---|
PMID | [PMID 23535033] |
Trait | Alzheimer's disease (cognitive decline) |
Title | Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. |
Risk Allele | |
P-val | 6E-7 |
Odds Ratio | .34 unit decrease |