rs10462023
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10462023(A;A) |
Make rs10462023(A;G) |
Make rs10462023(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 2 |
Position | 238275940 |
Gene | PER2 |
is a | snp |
is | mentioned by |
dbSNP | rs10462023 |
dbSNP (classic) | rs10462023 |
ClinGen | rs10462023 |
ebi | rs10462023 |
HLI | rs10462023 |
Exac | rs10462023 |
Gnomad | rs10462023 |
Varsome | rs10462023 |
LitVar | rs10462023 |
Map | rs10462023 |
PheGenI | rs10462023 |
Biobank | rs10462023 |
1000 genomes | rs10462023 |
hgdp | rs10462023 |
ensembl | rs10462023 |
geneview | rs10462023 |
scholar | rs10462023 |
rs10462023 | |
pharmgkb | rs10462023 |
gwascentral | rs10462023 |
openSNP | rs10462023 |
23andMe | rs10462023 |
SNPshot | rs10462023 |
SNPdbe | rs10462023 |
MSV3d | rs10462023 |
GWAS Ctlg | rs10462023 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25799324] Depression-associated ARNTL and PER2 genetic variants in psychotic disorders