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rs35866326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35866326(C;G)
Make rs35866326(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position57557163
is asnp
is mentioned by
dbSNPrs35866326
ebirs35866326
HLIrs35866326
Exacrs35866326
Varsomers35866326
Maprs35866326
PheGenIrs35866326
hapmaprs35866326
1000 genomesrs35866326
hgdprs35866326
ensemblrs35866326
gopubmedrs35866326
geneviewrs35866326
scholarrs35866326
googlers35866326
pharmgkbrs35866326
gwascentralrs35866326
openSNPrs35866326
23andMers35866326
23andMe allrs35866326
SNP Nexus

SNPshotrs35866326
SNPdbers35866326
MSV3drs35866326
GWAS Ctlgrs35866326
GMAF0.1685
Max Magnitude0
? (C;C) (C;G) (G;G) 28
Rs35866326
PubMed [PMID 16252231OA-icon.png]
Affy Probeset SNP_A-2127493
Affy Orientation reverse
On GW 5.0
Alleles A/B C/G
Ancestral
Population
Allele C
Case Freq. 0.93
Control Freq. 0.89
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.88
Disease Parkinson's disease (PKD)


rs35866326 increases susceptibility to Parkinson's disease 1.88 times for carriers of the C allele [PMID 16252231OA-icon.png]


[PMID 16685661OA-icon.png] Genomewide association, Parkinson disease, and PARK10.


[PMID 16685662OA-icon.png] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.


[PMID 16685663OA-icon.png] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.