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rs6963573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0
Make rs6963573(A;A)
Make rs6963573(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position36788795
is asnp
is mentioned by
dbSNPrs6963573
ebirs6963573
HLIrs6963573
Exacrs6963573
Varsomers6963573
Maprs6963573
PheGenIrs6963573
hapmaprs6963573
1000 genomesrs6963573
hgdprs6963573
ensemblrs6963573
gopubmedrs6963573
geneviewrs6963573
scholarrs6963573
googlers6963573
pharmgkbrs6963573
gwascentralrs6963573
openSNPrs6963573
23andMers6963573
23andMe allrs6963573
SNP Nexus

SNPshotrs6963573
SNPdbers6963573
MSV3drs6963573
GWAS Ctlgrs6963573
GMAF0.07713
Max Magnitude0
? (A;A) (A;G) (G;G) 28
Rs6963573
PubMed [PMID 16252231OA-icon.png]
Affy Probeset SNP_A-2183433
Affy Orientation reverse
On GW 5.0
Alleles A/B C/T
Ancestral G
Population
Allele A
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.71
Disease Parkinson's disease (PKD)


rs6963573 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.71 times for carriers of the A allele [PMID 16252231OA-icon.png]