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rs10200894

From SNPedia

Orientationplus
Stabilizedplus
Make rs10200894(C;C)
Make rs10200894(C;G)
Make rs10200894(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position227952416
is asnp
is mentioned by
dbSNPrs10200894
ebirs10200894
HLIrs10200894
Exacrs10200894
Varsomers10200894
Maprs10200894
PheGenIrs10200894
hapmaprs10200894
1000 genomesrs10200894
hgdprs10200894
ensemblrs10200894
gopubmedrs10200894
geneviewrs10200894
scholarrs10200894
googlers10200894
pharmgkbrs10200894
gwascentralrs10200894
openSNPrs10200894
23andMers10200894
23andMe allrs10200894
SNP Nexus

SNPshotrs10200894
SNPdbers10200894
MSV3drs10200894
GWAS Ctlgrs10200894
GMAF0.1754
Max Magnitude
? (C;C) (C;G) (G;G) 28
Rs10200894
PubMed [PMID 16252231OA-icon.png]
Affy Probeset SNP_A-8385601
Affy Orientation same
On GW 5.0
Alleles A/B C/G
Ancestral C
Population
Allele C
Case Freq. 0.93
Control Freq. 0.87
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.84
Disease Parkinson's disease (PKD)


rs10200894 increases susceptibility to Parkinson's disease 1.84 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.