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rs2245218

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0
Make rs2245218(A;A)
Make rs2245218(A;G)
Make rs2245218(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position13813331
GenePRDM2
is asnp
is mentioned by
dbSNPrs2245218
ebirs2245218
HLIrs2245218
Exacrs2245218
Varsomers2245218
Maprs2245218
PheGenIrs2245218
hapmaprs2245218
1000 genomesrs2245218
hgdprs2245218
ensemblrs2245218
gopubmedrs2245218
geneviewrs2245218
scholarrs2245218
googlers2245218
pharmgkbrs2245218
gwascentralrs2245218
openSNPrs2245218
23andMers2245218
23andMe allrs2245218
SNP Nexus

SNPshotrs2245218
SNPdbers2245218
MSV3drs2245218
GWAS Ctlgrs2245218
GMAF0.1685
Max Magnitude0
? (A;A) (A;G) (G;G) 28
rs2245218 increases susceptibility to Parkinson's disease 1.67 times for carriers of the G allele [PMID 16252231OA-icon.png]

[PMID 16685661OA-icon.png] Genomewide association, Parkinson disease, and PARK10.

[PMID 16685662OA-icon.png] No evidence for association with Parkinson disease for 13 single-nucleotide polymorphisms identified by whole-genome association screening.

[PMID 16685663OA-icon.png] A case-control association study of the 12 single-nucleotide polymorphisms implicated in Parkinson disease by a recent genome scan.