rs9378249
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs9378249(G;G) |
Make rs9378249(G;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31359924 |
is a | snp |
is | mentioned by |
dbSNP | rs9378249 |
dbSNP (classic) | rs9378249 |
ClinGen | rs9378249 |
ebi | rs9378249 |
HLI | rs9378249 |
Exac | rs9378249 |
Gnomad | rs9378249 |
Varsome | rs9378249 |
LitVar | rs9378249 |
Map | rs9378249 |
PheGenI | rs9378249 |
Biobank | rs9378249 |
1000 genomes | rs9378249 |
hgdp | rs9378249 |
ensembl | rs9378249 |
geneview | rs9378249 |
scholar | rs9378249 |
rs9378249 | |
pharmgkb | rs9378249 |
gwascentral | rs9378249 |
openSNP | rs9378249 |
23andMe | rs9378249 |
SNPshot | rs9378249 |
SNPdbe | rs9378249 |
MSV3d | rs9378249 |
GWAS Ctlg | rs9378249 |
GMAF | 0.07025 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21254220] |
Trait | |
Title | Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder. |
Risk Allele | |
P-val | 1E-8 |
Odds Ratio | None None |
[PMID 21291537] Evidence for somatic gene conversion and deletion in bipolar disorder, Crohn's disease, coronary artery disease, hypertension, rheumatoid arthritis, type-1 diabetes, and type-2 diabetes.