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rs9370399

From SNPedia

Orientationplus
Make rs9370399(A;A)
Make rs9370399(A;C)
Make rs9370399(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position55180227
GeneHCRTR2
is asnp
is mentioned by
dbSNPrs9370399
ebirs9370399
HLIrs9370399
Exacrs9370399
Varsomers9370399
Maprs9370399
PheGenIrs9370399
hapmaprs9370399
1000 genomesrs9370399
hgdprs9370399
ensemblrs9370399
gopubmedrs9370399
geneviewrs9370399
scholarrs9370399
googlers9370399
pharmgkbrs9370399
gwascentralrs9370399
openSNPrs9370399
23andMers9370399
23andMe allrs9370399
SNP Nexus

SNPshotrs9370399
SNPdbers9370399
MSV3drs9370399
GWAS Ctlgrs9370399
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 27335043] Lack of association between genetic polymorphism of circadian genes (PER2, PER3, CLOCK and OX2R) with late onset depression and Alzheimer's disease in a sample of a Brazilian population (Circadian Genes, Late-Onset Depression and Alzheimer's Disease).