rs13398848
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs13398848(A;G) |
Make rs13398848(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 84018044 |
is a | snp |
is | mentioned by |
dbSNP | rs13398848 |
dbSNP (classic) | rs13398848 |
ClinGen | rs13398848 |
ebi | rs13398848 |
HLI | rs13398848 |
Exac | rs13398848 |
Gnomad | rs13398848 |
Varsome | rs13398848 |
LitVar | rs13398848 |
Map | rs13398848 |
PheGenI | rs13398848 |
Biobank | rs13398848 |
1000 genomes | rs13398848 |
hgdp | rs13398848 |
ensembl | rs13398848 |
geneview | rs13398848 |
scholar | rs13398848 |
rs13398848 | |
pharmgkb | rs13398848 |
gwascentral | rs13398848 |
openSNP | rs13398848 |
23andMe | rs13398848 |
SNPshot | rs13398848 |
SNPdbe | rs13398848 |
MSV3d | rs13398848 |
GWAS Ctlg | rs13398848 |
GMAF | 0.08219 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20585324] |
Trait | Conduct disorder (case status) |
Title | Genome-wide association study of conduct disorder symptomatology |
Risk Allele | |
P-val | 0.000005 |
Odds Ratio | 1.59 [1.30-1.95] |