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rs10878226

From SNPedia

Orientationplus
Stabilizedplus
Make rs10878226(C;C)
Make rs10878226(C;G)
Make rs10878226(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position40223890
GeneLRRK2
is asnp
is mentioned by
dbSNPrs10878226
ebirs10878226
HLIrs10878226
Exacrs10878226
Varsomers10878226
Maprs10878226
PheGenIrs10878226
hapmaprs10878226
1000 genomesrs10878226
hgdprs10878226
ensemblrs10878226
gopubmedrs10878226
geneviewrs10878226
scholarrs10878226
googlers10878226
pharmgkbrs10878226
gwascentralrs10878226
openSNPrs10878226
23andMers10878226
23andMe allrs10878226
SNP Nexus

SNPshotrs10878226
SNPdbers10878226
MSV3drs10878226
GWAS Ctlgrs10878226
GMAF0.07208
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 23115130OA-icon.png] Common variation in the LRRK2 gene is a risk factor for Parkinson's disease