rs2697962

minus

Geno	Mag	Summary
(A;A)	2	Increased risk of developing Parkinson's Disease
(A;G)	1.5	Slightly increased risk of developing Parkinson's Disease
(C;C)	0
(G;G)	1	Normal risk of developing Parkinson's Disease

Reference

GRCh38 38.1/141

Chromosome

1

Position

13824497

Gene

PRDM2

is a	snp
is	mentioned by
dbSNP	rs2697962
dbSNP (classic)	rs2697962
ClinGen	rs2697962
ebi	rs2697962
HLI	rs2697962
Exac	rs2697962
Gnomad	rs2697962
Varsome	rs2697962
LitVar	rs2697962
Map	rs2697962
PheGenI	rs2697962
Biobank	rs2697962
1000 genomes	rs2697962
hgdp	rs2697962
ensembl	rs2697962
geneview	rs2697962
scholar	rs2697962
google	rs2697962
pharmgkb	rs2697962
gwascentral	rs2697962
openSNP	rs2697962
23andMe	rs2697962
SNPshot	rs2697962
SNPdbe	rs2697962
MSV3d	rs2697962
GWAS Ctlg	rs2697962

GMAF

0.1561

Max Magnitude

2

?

(A;A) (A;G) (G;G)

28

Rs2697962
PubMed	[PMID 16252231 ]
Affy Probeset	SNP_A-8401263
Affy Orientation	reverse
On GW 5.0
Alleles A/B	C/T
Ancestral	A
Population
Allele	A
Case Freq.
Control Freq.
Odds Ratio Het
Odds Ratio Hom
Odds Ratio All	1.67
Disease	Parkinson's disease (PKD)

rs2697962 is in linkage disequilibrium with a polymorphism that increases susceptibility to Parkinson's disease 1.67 times for carriers of the A allele [PMID 16252231 ]