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rs900147

From SNPedia

Orientationminus
Make rs900147(C;C)
Make rs900147(C;T)
Make rs900147(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position13272293
GeneLOC105376560
is asnp
is mentioned by
dbSNPrs900147
ebirs900147
HLIrs900147
Exacrs900147
Varsomers900147
Maprs900147
PheGenIrs900147
hapmaprs900147
1000 genomesrs900147
hgdprs900147
ensemblrs900147
gopubmedrs900147
geneviewrs900147
scholarrs900147
googlers900147
pharmgkbrs900147
gwascentralrs900147
openSNPrs900147
23andMers900147
23andMe allrs900147
SNP Nexus

SNPshotrs900147
SNPdbers900147
MSV3drs900147
GWAS Ctlgrs900147
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 26507264OA-icon.png] Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese