rs10900020
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10900020(A;A) |
Make rs10900020(A;T) |
Make rs10900020(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 44331749 |
Gene | CXCL12 |
is a | snp |
is | mentioned by |
dbSNP | rs10900020 |
dbSNP (classic) | rs10900020 |
ClinGen | rs10900020 |
ebi | rs10900020 |
HLI | rs10900020 |
Exac | rs10900020 |
Gnomad | rs10900020 |
Varsome | rs10900020 |
LitVar | rs10900020 |
Map | rs10900020 |
PheGenI | rs10900020 |
Biobank | rs10900020 |
1000 genomes | rs10900020 |
hgdp | rs10900020 |
ensembl | rs10900020 |
geneview | rs10900020 |
scholar | rs10900020 |
rs10900020 | |
pharmgkb | rs10900020 |
gwascentral | rs10900020 |
openSNP | rs10900020 |
23andMe | rs10900020 |
SNPshot | rs10900020 |
SNPdbe | rs10900020 |
MSV3d | rs10900020 |
GWAS Ctlg | rs10900020 |
GMAF | 0.07713 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 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 | 3E-6 |
Odds Ratio | .15 [NR] unit decrease |