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rs1223271

From SNPedia

Orientationplus
Stabilizedplus
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
(G;G) 1 Normal risk of developing Parkinson's Disease
ReferenceGRCh38 38.1/141
Chromosome20
Position13316265
is asnp
is mentioned by
dbSNPrs1223271
ebirs1223271
HLIrs1223271
Exacrs1223271
Varsomers1223271
Maprs1223271
PheGenIrs1223271
hapmaprs1223271
1000 genomesrs1223271
hgdprs1223271
ensemblrs1223271
gopubmedrs1223271
geneviewrs1223271
scholarrs1223271
googlers1223271
pharmgkbrs1223271
gwascentralrs1223271
openSNPrs1223271
23andMers1223271
23andMe allrs1223271
SNP Nexus

SNPshotrs1223271
SNPdbers1223271
MSV3drs1223271
GWAS Ctlgrs1223271
GMAF0.1892
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 A
P-val 0.000005
Odds Ratio 1.18 [NR]


GET Evidence
rs1223271
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.132812
summary