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rs356186

From SNPedia

Orientationplus
Stabilizedplus
Make rs356186(A;A)
Make rs356186(A;G)
Make rs356186(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position89784213
GeneSNCA
is asnp
is mentioned by
dbSNPrs356186
dbSNP (classic)rs356186
ClinGenrs356186
ebirs356186
HLIrs356186
Exacrs356186
Gnomadrs356186
Varsomers356186
LitVarrs356186
Maprs356186
PheGenIrs356186
Biobankrs356186
1000 genomesrs356186
hgdprs356186
ensemblrs356186
geneviewrs356186
scholarrs356186
googlers356186
pharmgkbrs356186
gwascentralrs356186
openSNPrs356186
23andMers356186
SNPshotrs356186
SNPdbers356186
MSV3drs356186
GWAS Ctlgrs356186
GMAF0.1703
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 22104010OA-icon.png] SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population


[PMID 15637659OA-icon.png] Linkage disequilibrium patterns and tagSNP transferability among European populations.


[PMID 19771175OA-icon.png] Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.


[PMID 25656566] Alpha-synuclein (SNCA) polymorphisms and susceptibility to Parkinson's disease: A meta-analysis


[PMID 30410434OA-icon.png] A Comprehensive Analysis of the Association Between SNCA Polymorphisms and the Risk of Parkinson's Disease.