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rs356229

From SNPedia

Orientationminus
Stabilizedminus
Make rs356229(A;A)
Make rs356229(A;G)
Make rs356229(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position89685446
is asnp
is mentioned by
dbSNPrs356229
ebirs356229
HLIrs356229
Exacrs356229
Varsomers356229
Maprs356229
PheGenIrs356229
hapmaprs356229
1000 genomesrs356229
hgdprs356229
ensemblrs356229
gopubmedrs356229
geneviewrs356229
scholarrs356229
googlers356229
pharmgkbrs356229
gwascentralrs356229
openSNPrs356229
23andMers356229
23andMe allrs356229
SNP Nexus

SNPshotrs356229
SNPdbers356229
MSV3drs356229
GWAS Ctlgrs356229
GMAF0.259
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 21058943OA-icon.png] Replication of GWAS associations for GAK and MAPT in Parkinson's disease


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


[PMID 18985386OA-icon.png] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.


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


[PMID 22425546] SNCA polymorphisms, smoking, and sporadic Parkinson's disease in Japanese.