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rs11737074

From SNPedia

Orientationplus
Stabilizedplus
Make rs11737074(A;A)
Make rs11737074(A;G)
Make rs11737074(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position124160218
is asnp
is mentioned by
dbSNPrs11737074
ebirs11737074
HLIrs11737074
Exacrs11737074
Varsomers11737074
Maprs11737074
PheGenIrs11737074
hapmaprs11737074
1000 genomesrs11737074
hgdprs11737074
ensemblrs11737074
gopubmedrs11737074
geneviewrs11737074
scholarrs11737074
googlers11737074
pharmgkbrs11737074
gwascentralrs11737074
openSNPrs11737074
23andMers11737074
23andMe allrs11737074
SNP Nexus

SNPshotrs11737074
SNPdbers11737074
MSV3drs11737074
GWAS Ctlgrs11737074
GMAF0.14
Max Magnitude
? (A;A) (A;G) (G;G) 28

rs11737074 increases susceptibility to Parkinson's disease 1.50 times for carriers of the A 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.