rs253959
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs253959(A;A) |
Make rs253959(A;G) |
Make rs253959(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 116233060 |
Gene | COMMD10 |
is a | snp |
is | mentioned by |
dbSNP | rs253959 |
dbSNP (classic) | rs253959 |
ClinGen | rs253959 |
ebi | rs253959 |
HLI | rs253959 |
Exac | rs253959 |
Gnomad | rs253959 |
Varsome | rs253959 |
LitVar | rs253959 |
Map | rs253959 |
PheGenI | rs253959 |
Biobank | rs253959 |
1000 genomes | rs253959 |
hgdp | rs253959 |
ensembl | rs253959 |
geneview | rs253959 |
scholar | rs253959 |
rs253959 | |
pharmgkb | rs253959 |
gwascentral | rs253959 |
openSNP | rs253959 |
23andMe | rs253959 |
SNPshot | rs253959 |
SNPdbe | rs253959 |
MSV3d | rs253959 |
GWAS Ctlg | rs253959 |
GMAF | 0.4656 |
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 | T |
P-val | 0.000008 |
Odds Ratio | 1.2100 None |