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rs199533

From SNPedia

Orientationminus
Stabilizedminus
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
Chromosome17
Position46751565
GeneNSF
is asnp
is mentioned by
dbSNPrs199533
ebirs199533
HLIrs199533
Exacrs199533
Varsomers199533
Maprs199533
PheGenIrs199533
hapmaprs199533
1000 genomesrs199533
hgdprs199533
ensemblrs199533
gopubmedrs199533
geneviewrs199533
scholarrs199533
googlers199533
pharmgkbrs199533
gwascentralrs199533
openSNPrs199533
23andMers199533
23andMe allrs199533
SNP Nexus

SNPshotrs199533
SNPdbers199533
MSV3drs199533
GWAS Ctlgrs199533
GMAF0.1084
Max Magnitude2
? (C;C) (C;T) (T;T) 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 T
P-val 1E-14
Odds Ratio 1.28 [NR]
GWAS snp
PMID [PMID 20711177OA-icon.png]
Trait
Title Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
Risk Allele C
P-val 0.000001
Odds Ratio 1.35 [1.19-1.52]