rs7581919
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common on affy axiom data |
Make rs7581919(C;C) |
Make rs7581919(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 15524632 |
Gene | NBAS |
is a | snp |
is | mentioned by |
dbSNP | rs7581919 |
dbSNP (classic) | rs7581919 |
ClinGen | rs7581919 |
ebi | rs7581919 |
HLI | rs7581919 |
Exac | rs7581919 |
Gnomad | rs7581919 |
Varsome | rs7581919 |
LitVar | rs7581919 |
Map | rs7581919 |
PheGenI | rs7581919 |
Biobank | rs7581919 |
1000 genomes | rs7581919 |
hgdp | rs7581919 |
ensembl | rs7581919 |
geneview | rs7581919 |
scholar | rs7581919 |
rs7581919 | |
pharmgkb | rs7581919 |
gwascentral | rs7581919 |
openSNP | rs7581919 |
23andMe | rs7581919 |
SNPshot | rs7581919 |
SNPdbe | rs7581919 |
MSV3d | rs7581919 |
GWAS Ctlg | rs7581919 |
GMAF | 0.01837 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324] |
Trait | Conduct disorder (case status) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000008 |
Odds Ratio | 1.85 [1.41-2.43] |