rs2058710
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2058710(A;A) |
Make rs2058710(A;G) |
Make rs2058710(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 206257058 |
Gene | GPR1-AS |
is a | snp |
is | mentioned by |
dbSNP | rs2058710 |
dbSNP (classic) | rs2058710 |
ClinGen | rs2058710 |
ebi | rs2058710 |
HLI | rs2058710 |
Exac | rs2058710 |
Gnomad | rs2058710 |
Varsome | rs2058710 |
LitVar | rs2058710 |
Map | rs2058710 |
PheGenI | rs2058710 |
Biobank | rs2058710 |
1000 genomes | rs2058710 |
hgdp | rs2058710 |
ensembl | rs2058710 |
geneview | rs2058710 |
scholar | rs2058710 |
rs2058710 | |
pharmgkb | rs2058710 |
gwascentral | rs2058710 |
openSNP | rs2058710 |
23andMe | rs2058710 |
SNPshot | rs2058710 |
SNPdbe | rs2058710 |
MSV3d | rs2058710 |
GWAS Ctlg | rs2058710 |
GMAF | 0.2084 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22688191] |
Trait | |
Title | Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. |
Risk Allele | A |
P-val | 0.000009 |
Odds Ratio | 1.2400 None |