rs12063142

Orientation

plus

Stabilized

plus

Make rs12063142(C;C)

Make rs12063142(C;T)

Make rs12063142(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

18813023

is a	snp
is	mentioned by
dbSNP	rs12063142
dbSNP (classic)	rs12063142
ClinGen	rs12063142
ebi	rs12063142
HLI	rs12063142
Exac	rs12063142
Gnomad	rs12063142
Varsome	rs12063142
LitVar	rs12063142
Map	rs12063142
PheGenI	rs12063142
Biobank	rs12063142
1000 genomes	rs12063142
hgdp	rs12063142
ensembl	rs12063142
geneview	rs12063142
scholar	rs12063142
google	rs12063142
pharmgkb	rs12063142
gwascentral	rs12063142
openSNP	rs12063142
23andMe	rs12063142
SNPshot	rs12063142
SNPdbe	rs12063142
MSV3d	rs12063142
GWAS Ctlg	rs12063142

GMAF

0.2052

Max Magnitude

0

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

GWAS snp
PMID	[PMID 20070850]
Trait	Parkinson's disease
Title	Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
Risk Allele
P-val	5E-7
Odds Ratio	None None