rs9917256

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in complete genomics

Make rs9917256(A;A)

Make rs9917256(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

168286525

is a	snp
is	mentioned by
dbSNP	rs9917256
dbSNP (classic)	rs9917256
ClinGen	rs9917256
ebi	rs9917256
HLI	rs9917256
Exac	rs9917256
Gnomad	rs9917256
Varsome	rs9917256
LitVar	rs9917256
Map	rs9917256
PheGenI	rs9917256
Biobank	rs9917256
1000 genomes	rs9917256
hgdp	rs9917256
ensembl	rs9917256
geneview	rs9917256
scholar	rs9917256
google	rs9917256
pharmgkb	rs9917256
gwascentral	rs9917256
openSNP	rs9917256
23andMe	rs9917256
SNPshot	rs9917256
SNPdbe	rs9917256
MSV3d	rs9917256
GWAS Ctlg	rs9917256

GMAF

0.1869

Max Magnitude

0

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

GWAS snp
PMID	[PMID 22451204]
Trait
Title	Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Risk Allele
P-val	0.000003
Odds Ratio	1.1900 None