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rs5998557

From SNPedia

Orientationplus
Stabilizedplus
Make rs5998557(C;C)
Make rs5998557(C;G)
Make rs5998557(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position32611052
GeneSYN3
is asnp
is mentioned by
dbSNPrs5998557
ebirs5998557
HLIrs5998557
Exacrs5998557
Varsomers5998557
Maprs5998557
PheGenIrs5998557
hapmaprs5998557
1000 genomesrs5998557
hgdprs5998557
ensemblrs5998557
gopubmedrs5998557
geneviewrs5998557
scholarrs5998557
googlers5998557
pharmgkbrs5998557
gwascentralrs5998557
openSNPrs5998557
23andMers5998557
23andMe allrs5998557
SNP Nexus

SNPshotrs5998557
SNPdbers5998557
MSV3drs5998557
GWAS Ctlgrs5998557
GMAF0.3701
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 24586301OA-icon.png] No Association of Four Candidate Genetic Variants in MnSOD and SYNIII with Parkinson's Disease in Two Chinese Populations