rs10789369
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10789369(A;A) |
Make rs10789369(A;G) |
Make rs10789369(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 73359226 |
is a | snp |
is | mentioned by |
dbSNP | rs10789369 |
dbSNP (classic) | rs10789369 |
ClinGen | rs10789369 |
ebi | rs10789369 |
HLI | rs10789369 |
Exac | rs10789369 |
Gnomad | rs10789369 |
Varsome | rs10789369 |
LitVar | rs10789369 |
Map | rs10789369 |
PheGenI | rs10789369 |
Biobank | rs10789369 |
1000 genomes | rs10789369 |
hgdp | rs10789369 |
ensembl | rs10789369 |
geneview | rs10789369 |
scholar | rs10789369 |
rs10789369 | |
pharmgkb | rs10789369 |
gwascentral | rs10789369 |
openSNP | rs10789369 |
23andMe | rs10789369 |
SNPshot | rs10789369 |
SNPdbe | rs10789369 |
MSV3d | rs10789369 |
GWAS Ctlg | rs10789369 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23974872] |
Trait | Schizophrenia |
Title | Genome-wide association analysis identifies 13 new risk loci for schizophrenia. |
Risk Allele | A |
P-val | 4E-10 |
Odds Ratio | 1.10 [1.07-1.12] |