rs6532197

Orientation

plus

Stabilized

plus

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

Reference

GRCh38 38.1/141

Chromosome

4

Position

89876150

is a	snp
is	mentioned by
dbSNP	rs6532197
dbSNP (classic)	rs6532197
ClinGen	rs6532197
ebi	rs6532197
HLI	rs6532197
Exac	rs6532197
Gnomad	rs6532197
Varsome	rs6532197
LitVar	rs6532197
Map	rs6532197
PheGenI	rs6532197
Biobank	rs6532197
1000 genomes	rs6532197
hgdp	rs6532197
ensembl	rs6532197
geneview	rs6532197
scholar	rs6532197
google	rs6532197
pharmgkb	rs6532197
gwascentral	rs6532197
openSNP	rs6532197
23andMe	rs6532197
SNPshot	rs6532197
SNPdbe	rs6532197
MSV3d	rs6532197
GWAS Ctlg	rs6532197

GMAF

0.2029

Max Magnitude

2

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 19915575]
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]