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rs11155313

From SNPedia

Orientationplus
Stabilizedplus
Make rs11155313(A;A)
Make rs11155313(A;G)
Make rs11155313(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position143640440
GenePHACTR2
is asnp
is mentioned by
dbSNPrs11155313
ebirs11155313
HLIrs11155313
Exacrs11155313
Varsomers11155313
Maprs11155313
PheGenIrs11155313
hapmaprs11155313
1000 genomesrs11155313
hgdprs11155313
ensemblrs11155313
gopubmedrs11155313
geneviewrs11155313
scholarrs11155313
googlers11155313
pharmgkbrs11155313
gwascentralrs11155313
openSNPrs11155313
23andMers11155313
23andMe allrs11155313
SNP Nexus

SNPshotrs11155313
SNPdbers11155313
MSV3drs11155313
GWAS Ctlgrs11155313
GMAF0.2525
Max Magnitude
? (A;A) (A;G) (G;G) 28

Four case-control series were combined along with previous GWAS results, yielding a 1.3x increased risk for Parkinson's disease among rs11155313 minor allele carriers.[PMID 19429005OA-icon.png]


[PMID 16252231OA-icon.png] High-resolution whole-genome association study of Parkinson disease.