rs2134294
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2134294(C;C) |
Make rs2134294(C;T) |
Make rs2134294(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 55269449 |
Gene | HCRTR2 |
is a | snp |
is | mentioned by |
dbSNP | rs2134294 |
dbSNP (classic) | rs2134294 |
ClinGen | rs2134294 |
ebi | rs2134294 |
HLI | rs2134294 |
Exac | rs2134294 |
Gnomad | rs2134294 |
Varsome | rs2134294 |
LitVar | rs2134294 |
Map | rs2134294 |
PheGenI | rs2134294 |
Biobank | rs2134294 |
1000 genomes | rs2134294 |
hgdp | rs2134294 |
ensembl | rs2134294 |
geneview | rs2134294 |
scholar | rs2134294 |
rs2134294 | |
pharmgkb | rs2134294 |
gwascentral | rs2134294 |
openSNP | rs2134294 |
23andMe | rs2134294 |
SNPshot | rs2134294 |
SNPdbe | rs2134294 |
MSV3d | rs2134294 |
GWAS Ctlg | rs2134294 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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).