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rs1438852

From SNPedia

Orientationplus
Stabilizedplus
Make rs1438852(C;C)
Make rs1438852(C;T)
Make rs1438852(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position118838515
is asnp
is mentioned by
dbSNPrs1438852
ebirs1438852
HLIrs1438852
Exacrs1438852
Varsomers1438852
Maprs1438852
PheGenIrs1438852
hapmaprs1438852
1000 genomesrs1438852
hgdprs1438852
ensemblrs1438852
gopubmedrs1438852
geneviewrs1438852
scholarrs1438852
googlers1438852
pharmgkbrs1438852
gwascentralrs1438852
openSNPrs1438852
23andMers1438852
23andMe allrs1438852
SNP Nexus

SNPshotrs1438852
SNPdbers1438852
MSV3drs1438852
GWAS Ctlgrs1438852
GMAF0.4853
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19345444] Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson's disease.