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rs181489

From SNPedia

Orientationplus
Stabilizedplus
Make rs181489(C;C)
Make rs181489(C;T)
Make rs181489(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position89713869
is asnp
is mentioned by
dbSNPrs181489
ebirs181489
HLIrs181489
Exacrs181489
Varsomers181489
Maprs181489
PheGenIrs181489
hapmaprs181489
1000 genomesrs181489
hgdprs181489
ensemblrs181489
gopubmedrs181489
geneviewrs181489
scholarrs181489
googlers181489
pharmgkbrs181489
gwascentralrs181489
openSNPrs181489
23andMers181489
23andMe allrs181489
SNP Nexus

SNPshotrs181489
SNPdbers181489
MSV3drs181489
GWAS Ctlgrs181489
GMAF0.1979
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23962496OA-icon.png] The protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants


[PMID 21391235OA-icon.png] Independent and joint effects of the MAPT and SNCA genes in Parkinson disease.


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