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rs6847679

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs6847679(C;C)
Make rs6847679(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position137841472
is asnp
is mentioned by
dbSNPrs6847679
ebirs6847679
HLIrs6847679
Exacrs6847679
Varsomers6847679
Maprs6847679
PheGenIrs6847679
hapmaprs6847679
1000 genomesrs6847679
hgdprs6847679
ensemblrs6847679
gopubmedrs6847679
geneviewrs6847679
scholarrs6847679
googlers6847679
pharmgkbrs6847679
gwascentralrs6847679
openSNPrs6847679
23andMers6847679
23andMe allrs6847679
SNP Nexus

SNPshotrs6847679
SNPdbers6847679
MSV3drs6847679
GWAS Ctlgrs6847679
GMAF0.09458
Max Magnitude0
? (C;C) (C;T) (T;T) 28
Rs6847679
PubMed [PMID 16252231OA-icon.png]
Affy Probeset SNP_A-4154756
Affy Orientation same
On GW 5.0
Alleles A/B C/T
Ancestral T
Population
Allele C
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.71
Disease Parkinson's disease (PKD)


rs6847679 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.71 times for carriers of the C allele [PMID 16252231OA-icon.png]