rs199533

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

17

Position

46751565

Gene

NSF

is a	snp
is	mentioned by
dbSNP	rs199533
dbSNP (classic)	rs199533
ClinGen	rs199533
ebi	rs199533
HLI	rs199533
Exac	rs199533
Gnomad	rs199533
Varsome	rs199533
LitVar	rs199533
Map	rs199533
PheGenI	rs199533
Biobank	rs199533
1000 genomes	rs199533
hgdp	rs199533
ensembl	rs199533
geneview	rs199533
scholar	rs199533
google	rs199533
pharmgkb	rs199533
gwascentral	rs199533
openSNP	rs199533
23andMe	rs199533
SNPshot	rs199533
SNPdbe	rs199533
MSV3d	rs199533
GWAS Ctlg	rs199533

GMAF

0.1084

Max Magnitude

2

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 19915575]
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 20711177]
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]