Rs10200894

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is asnp
is mentioned by
dbSNPrs10200894
hapmaprs10200894
hgdprs10200894
ensemblrs10200894
gopubmedrs10200894
scholarrs10200894
googlers10200894
pharmgkbrs10200894
hgvbaseg2prs10200894
medrefsnprs10200894
23andMers10200894
SNP Nexus

Chromosome2
Orientationplus
Position228525375
GenotypeEffect
rs10200894(C;C)*?
rs10200894(C;G)*?
rs10200894(G;G)*?


Rs10200894
PubMed [PMID 16252231]
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)
? (C;C) (C;G) (G;G)

rs10200894 increases susceptibility to Parkinson's disease 1.84 times for carriers of the C allele [PMID 16252231]

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