rs2823357
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2823357(A;A) |
Make rs2823357(A;G) |
Make rs2823357(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 21 |
Position | 15542586 |
Gene | LOC105369302 |
is a | snp |
is | mentioned by |
dbSNP | rs2823357 |
dbSNP (classic) | rs2823357 |
ClinGen | rs2823357 |
ebi | rs2823357 |
HLI | rs2823357 |
Exac | rs2823357 |
Gnomad | rs2823357 |
Varsome | rs2823357 |
LitVar | rs2823357 |
Map | rs2823357 |
PheGenI | rs2823357 |
Biobank | rs2823357 |
1000 genomes | rs2823357 |
hgdp | rs2823357 |
ensembl | rs2823357 |
geneview | rs2823357 |
scholar | rs2823357 |
rs2823357 | |
pharmgkb | rs2823357 |
gwascentral | rs2823357 |
openSNP | rs2823357 |
23andMe | rs2823357 |
SNPshot | rs2823357 |
SNPdbe | rs2823357 |
MSV3d | rs2823357 |
GWAS Ctlg | rs2823357 |
GMAF | 0.4601 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21738487] |
Trait | |
Title | Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. |
Risk Allele | A |
P-val | 6E-7 |
Odds Ratio | 1.1500 [1.09-1.21] |
[PMID 25929833] Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder