Have questions? Visit https://www.reddit.com/r/SNPedia

rs2823357

From SNPedia

Orientationplus
Stabilizedplus
Make rs2823357(A;A)
Make rs2823357(A;G)
Make rs2823357(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position15542586
is asnp
is mentioned by
dbSNPrs2823357
ebirs2823357
HLIrs2823357
Exacrs2823357
Varsomers2823357
Maprs2823357
PheGenIrs2823357
hapmaprs2823357
1000 genomesrs2823357
hgdprs2823357
ensemblrs2823357
gopubmedrs2823357
geneviewrs2823357
scholarrs2823357
googlers2823357
pharmgkbrs2823357
gwascentralrs2823357
openSNPrs2823357
23andMers2823357
23andMe allrs2823357
SNP Nexus

SNPshotrs2823357
SNPdbers2823357
MSV3drs2823357
GWAS Ctlgrs2823357
GMAF0.4601
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21738487OA-icon.png]
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