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rs356182

From SNPedia

Orientationminus
Geno Mag Summary
(C;C)
Make rs356182(C;T)
Make rs356182(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position89704960
GeneLOC105377329
is asnp
is mentioned by
dbSNPrs356182
ClinGenrs356182
ebirs356182
HLIrs356182
Exacrs356182
Varsomers356182
Maprs356182
PheGenIrs356182
hapmaprs356182
1000 genomesrs356182
hgdprs356182
ensemblrs356182
gopubmedrs356182
geneviewrs356182
scholarrs356182
googlers356182
pharmgkbrs356182
gwascentralrs356182
openSNPrs356182
23andMers356182
23andMe allrs356182
SNP Nexus

SNPshotrs356182
SNPdbers356182
MSV3drs356182
GWAS Ctlgrs356182
Max Magnitude
http://medicalxpress.com/news/2016-04-uncovers-genetic-variation-physical-decline.html parkinson's disease


[PMID 27538639] SNCA rs356182 variant increases risk of sporadic Parkinson's disease in ethnic Chinese.