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rs7684318

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7684318(C;C)
Make rs7684318(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position89733852
GeneSNCA
is asnp
is mentioned by
dbSNPrs7684318
ebirs7684318
HLIrs7684318
Exacrs7684318
Varsomers7684318
Maprs7684318
PheGenIrs7684318
hapmaprs7684318
1000 genomesrs7684318
hgdprs7684318
ensemblrs7684318
gopubmedrs7684318
geneviewrs7684318
scholarrs7684318
googlers7684318
pharmgkbrs7684318
gwascentralrs7684318
openSNPrs7684318
23andMers7684318
23andMe allrs7684318
SNP Nexus

SNPshotrs7684318
SNPdbers7684318
MSV3drs7684318
GWAS Ctlgrs7684318
GMAF0.303
Max Magnitude0

[PMID 20513365] SNP rs7684318 of the alpha-synuclein gene is associated with Parkinson's disease in the Han Chinese population

The risk allele appears to be C. [PMID 2051336]


[PMID 16500997] Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.


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