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rs1509269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs1509269(C;T)
Make rs1509269(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position137832570
is asnp
is mentioned by
dbSNPrs1509269
ebirs1509269
HLIrs1509269
Exacrs1509269
Varsomers1509269
Maprs1509269
PheGenIrs1509269
hapmaprs1509269
1000 genomesrs1509269
hgdprs1509269
ensemblrs1509269
gopubmedrs1509269
geneviewrs1509269
scholarrs1509269
googlers1509269
pharmgkbrs1509269
gwascentralrs1509269
openSNPrs1509269
23andMers1509269
23andMe allrs1509269
SNP Nexus

SNPshotrs1509269
SNPdbers1509269
MSV3drs1509269
GWAS Ctlgrs1509269
GMAF0.09458
Max Magnitude0
? (C;C) (C;T) (T;T) 28

rs1509269 increases susceptibility to Parkinson's disease 1.71 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.