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rs9917256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs9917256(A;A)
Make rs9917256(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position168286525
is asnp
is mentioned by
dbSNPrs9917256
ebirs9917256
HLIrs9917256
Exacrs9917256
Varsomers9917256
Maprs9917256
PheGenIrs9917256
hapmaprs9917256
1000 genomesrs9917256
hgdprs9917256
ensemblrs9917256
gopubmedrs9917256
geneviewrs9917256
scholarrs9917256
googlers9917256
pharmgkbrs9917256
gwascentralrs9917256
openSNPrs9917256
23andMers9917256
23andMe allrs9917256
SNP Nexus

SNPshotrs9917256
SNPdbers9917256
MSV3drs9917256
GWAS Ctlgrs9917256
GMAF0.1869
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22451204OA-icon.png]
Trait
Title Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Risk Allele
P-val 0.000003
Odds Ratio 1.1900 None