rs2910032
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2910032(C;C) |
Make rs2910032(C;T) |
Make rs2910032(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 153160794 |
is a | snp |
is | mentioned by |
dbSNP | rs2910032 |
dbSNP (classic) | rs2910032 |
ClinGen | rs2910032 |
ebi | rs2910032 |
HLI | rs2910032 |
Exac | rs2910032 |
Gnomad | rs2910032 |
Varsome | rs2910032 |
LitVar | rs2910032 |
Map | rs2910032 |
PheGenI | rs2910032 |
Biobank | rs2910032 |
1000 genomes | rs2910032 |
hgdp | rs2910032 |
ensembl | rs2910032 |
geneview | rs2910032 |
scholar | rs2910032 |
rs2910032 | |
pharmgkb | rs2910032 |
gwascentral | rs2910032 |
openSNP | rs2910032 |
23andMe | rs2910032 |
SNPshot | rs2910032 |
SNPdbe | rs2910032 |
MSV3d | rs2910032 |
GWAS Ctlg | rs2910032 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23974872] |
Trait | Schizophrenia |
Title | Genome-wide association analysis identifies 13 new risk loci for schizophrenia. |
Risk Allele | C |
P-val | 4E-8 |
Odds Ratio | 1.08 [1.05-1.11] |