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rs6896702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 1 Normal risk of developing Parkinson's Disease
(C;T) 1.5 Slightly increased risk of developing Parkinson's Disease
(T;T) 2 Increased risk of developing Parkinson's Disease
ReferenceGRCh38 38.1/141
Chromosome5
Position9331736
GeneSEMA5A
is asnp
is mentioned by
dbSNPrs6896702
ebirs6896702
HLIrs6896702
Exacrs6896702
Varsomers6896702
Maprs6896702
PheGenIrs6896702
hapmaprs6896702
1000 genomesrs6896702
hgdprs6896702
ensemblrs6896702
gopubmedrs6896702
geneviewrs6896702
scholarrs6896702
googlers6896702
pharmgkbrs6896702
gwascentralrs6896702
openSNPrs6896702
23andMers6896702
23andMe allrs6896702
SNP Nexus

SNPshotrs6896702
SNPdbers6896702
MSV3drs6896702
GWAS Ctlgrs6896702
GMAF0.3219
Max Magnitude2
? (C;C) (C;T) (T;T) 28
Rs6896702
PubMed [PMID 16252231OA-icon.png]
Affy Probeset SNP_A-8488227
Affy Orientation reverse
On GW 5.0
Alleles A/B A/G
Ancestral C
Population
Allele T
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All 1.74
Disease Parkinson's disease (PKD)


rs6896702 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.74 times for carriers of the T allele [PMID 16252231OA-icon.png]

Neighborrs7702187
Distance433