Rs1480597

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Orientationminus
is asnp
is mentioned by
dbSNPrs1480597
PheGenIrs1480597
nextbiors1480597
hapmaprs1480597
1000 genomesrs1480597
hgdprs1480597
ensemblrs1480597
gopubmedrs1480597
geneviewrs1480597
scholarrs1480597
googlers1480597
pharmgkbrs1480597
gwascentralrs1480597
openSNPrs1480597
23andMers1480597
23andMe allrs1480597
SNP Nexus

SNPshotrs1480597
SNPdbers1480597
MSV3drs1480597
Chromosome10
Orientationminus
GMAF0.1006
Position45161109
ReferenceGRCh37 37.1/131
Max Magnitude0
Geno Mag Summary
(G;G) 0
Make rs1480597(A;A)
Make rs1480597(A;G)
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs1480597
PubMedID [PMID 17052657]
Condition Parkinson's disease
Gene Intergenic
Risk Allele
pValue 2.00E-006
OR 2.5
95% CI 1.67-3.33



[PMID 19134182OA-icon.png] MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study.


[PMID 20823317OA-icon.png] is-rSNP: a novel technique for in silico regulatory SNP detection.


GET Evidence
rs1480597
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0703125
summary