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rs2102808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2102808(G;T)
Make rs2102808(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position168260515
is asnp
is mentioned by
dbSNPrs2102808
ebirs2102808
HLIrs2102808
Exacrs2102808
Varsomers2102808
Maprs2102808
PheGenIrs2102808
hapmaprs2102808
1000 genomesrs2102808
hgdprs2102808
ensemblrs2102808
gopubmedrs2102808
geneviewrs2102808
scholarrs2102808
googlers2102808
pharmgkbrs2102808
gwascentralrs2102808
openSNPrs2102808
23andMers2102808
23andMe allrs2102808
SNP Nexus

SNPshotrs2102808
SNPdbers2102808
MSV3drs2102808
GWAS Ctlgrs2102808
GMAF0.202
Max Magnitude0
GWAS snp
PMID [PMID 21292315OA-icon.png]
Trait
Title Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Risk Allele C
P-val 4E-10
Odds Ratio 1.1800 [1.12-1.24]