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rs17329669

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs17329669(A;G)
Make rs17329669(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position36812324
is asnp
is mentioned by
dbSNPrs17329669
ebirs17329669
HLIrs17329669
Exacrs17329669
Varsomers17329669
Maprs17329669
PheGenIrs17329669
hapmaprs17329669
1000 genomesrs17329669
hgdprs17329669
ensemblrs17329669
gopubmedrs17329669
geneviewrs17329669
scholarrs17329669
googlers17329669
pharmgkbrs17329669
gwascentralrs17329669
openSNPrs17329669
23andMers17329669
23andMe allrs17329669
SNP Nexus

SNPshotrs17329669
SNPdbers17329669
MSV3drs17329669
GWAS Ctlgrs17329669
GMAF0.07668
Max Magnitude0
? (A;A) (A;G) (G;G) 28

rs17329669 is an intergenic SNP on chromosome 7 between the AOAH gene and the ELMO1 gene (genes involved in neutrophils / possibly immune related).

rs17329669 (G) was associated with Parkinson's disease in a discordant sibling study [PMID 16252231OA-icon.png]

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

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