rs1351267
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1351267(A;A) |
Make rs1351267(A;G) |
Make rs1351267(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 152045912 |
is a | snp |
is | mentioned by |
dbSNP | rs1351267 |
dbSNP (classic) | rs1351267 |
ClinGen | rs1351267 |
ebi | rs1351267 |
HLI | rs1351267 |
Exac | rs1351267 |
Gnomad | rs1351267 |
Varsome | rs1351267 |
LitVar | rs1351267 |
Map | rs1351267 |
PheGenI | rs1351267 |
Biobank | rs1351267 |
1000 genomes | rs1351267 |
hgdp | rs1351267 |
ensembl | rs1351267 |
geneview | rs1351267 |
scholar | rs1351267 |
rs1351267 | |
pharmgkb | rs1351267 |
gwascentral | rs1351267 |
openSNP | rs1351267 |
23andMe | rs1351267 |
SNPshot | rs1351267 |
SNPdbe | rs1351267 |
MSV3d | rs1351267 |
GWAS Ctlg | rs1351267 |
GMAF | 0.4486 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23212062![]() |
Trait | Schizophrenia |
Title | Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. |
Risk Allele | |
P-val | 7E-6 |
Odds Ratio | .09 [NR] unit increase |