| Geno
|
Mag
|
Summary
|
| (C;C)
|
0
|
common in complete genomics
|
| Rs16851009
|
| PubMed
|
[PMID 16252231 ]
|
| Affy Probeset
|
SNP_A-8294813
|
| Affy Orientation
|
reverse
|
| On GW 5.0
|
|
| Alleles A/B
|
A/G
|
| Ancestral
|
C
|
| Population
|
|
| Allele
|
T
|
| Case Freq.
|
0.13
|
| Control Freq.
|
0.08
|
| Odds Ratio Het
|
|
| Odds Ratio Hom
|
|
| Odds Ratio All
|
1.84
|
| Disease
|
Parkinson's disease (PKD)
|
rs16851009 increases susceptibility to Parkinson's disease 1.84 times for carriers of the T allele [PMID 16252231]
[PMID 16685661] Genomewide association, Parkinson disease, and PARK10.
[PMID 16685662] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.
[PMID 16685663] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.
]
