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rs2697962

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 2 Increased risk of developing Parkinson's Disease
(A;G) 1.5 Slightly increased risk of developing Parkinson's Disease
(C;C) 0
(G;G) 1 Normal risk of developing Parkinson's Disease
ReferenceGRCh38 38.1/141
Chromosome1
Position13824497
GenePRDM2
is asnp
is mentioned by
dbSNPrs2697962
dbSNP (old)rs2697962
ClinGenrs2697962
ebirs2697962
HLIrs2697962
Exacrs2697962
Varsomers2697962
Maprs2697962
PheGenIrs2697962
Biobankrs2697962
1000 genomesrs2697962
hgdprs2697962
ensemblrs2697962
gopubmedrs2697962
geneviewrs2697962
scholarrs2697962
googlers2697962
pharmgkbrs2697962
gwascentralrs2697962
openSNPrs2697962
23andMers2697962
23andMe allrs2697962
SNP Nexus

SNPshotrs2697962
SNPdbers2697962
MSV3drs2697962
GWAS Ctlgrs2697962
GMAF0.1561
Max Magnitude2
? (A;A) (A;G) (G;G) 28
Rs2697962
PubMed [PMID 16252231OA-icon.png]
Affy Probeset SNP_A-8401263
Affy Orientation reverse
On GW 5.0
Alleles A/B C/T
Ancestral A
Population
Allele A
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.67
Disease Parkinson's disease (PKD)


rs2697962 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.67 times for carriers of the A allele [PMID 16252231OA-icon.png]