rs75617873
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common genotype |
Make rs75617873(A;C) |
Make rs75617873(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 44130225 |
Gene | PARVB |
is a | snp |
is | mentioned by |
dbSNP | rs75617873 |
dbSNP (classic) | rs75617873 |
ClinGen | rs75617873 |
ebi | rs75617873 |
HLI | rs75617873 |
Exac | rs75617873 |
Gnomad | rs75617873 |
Varsome | rs75617873 |
LitVar | rs75617873 |
Map | rs75617873 |
PheGenI | rs75617873 |
Biobank | rs75617873 |
1000 genomes | rs75617873 |
hgdp | rs75617873 |
ensembl | rs75617873 |
geneview | rs75617873 |
scholar | rs75617873 |
rs75617873 | |
pharmgkb | rs75617873 |
gwascentral | rs75617873 |
openSNP | rs75617873 |
23andMe | rs75617873 |
SNPshot | rs75617873 |
SNPdbe | rs75617873 |
MSV3d | rs75617873 |
GWAS Ctlg | rs75617873 |
GMAF | 0.01837 |
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 | 5E-7 |
Odds Ratio | .17 unit decrease |