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rs6532197

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1 Normal risk of developing Parkinson's Disease
(A;G) 1.5 Slightly increased risk of developing Parkinson's Disease
(G;G) 2 Increased risk of developing Parkinson's Disease
ReferenceGRCh38 38.1/141
Chromosome4
Position89876150
is asnp
is mentioned by
dbSNPrs6532197
ebirs6532197
HLIrs6532197
Exacrs6532197
Varsomers6532197
Maprs6532197
PheGenIrs6532197
hapmaprs6532197
1000 genomesrs6532197
hgdprs6532197
ensemblrs6532197
gopubmedrs6532197
geneviewrs6532197
scholarrs6532197
googlers6532197
pharmgkbrs6532197
gwascentralrs6532197
openSNPrs6532197
23andMers6532197
23andMe allrs6532197
SNP Nexus

SNPshotrs6532197
SNPdbers6532197
MSV3drs6532197
GWAS Ctlgrs6532197
GMAF0.2029
Max Magnitude2
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19915575OA-icon.png]
Trait Parkinson's disease
Title Genome-wide association study reveals genetic risk underlying Parkinson's disease
Risk Allele G
P-val 1E-7
Odds Ratio 1.32 [NR]


GET Evidence
rs6532197
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.226562
summary