rs6427356
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6427356(A;A) |
Make rs6427356(A;G) |
Make rs6427356(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 157160775 |
is a | snp |
is | mentioned by |
dbSNP | rs6427356 |
dbSNP (classic) | rs6427356 |
ClinGen | rs6427356 |
ebi | rs6427356 |
HLI | rs6427356 |
Exac | rs6427356 |
Gnomad | rs6427356 |
Varsome | rs6427356 |
LitVar | rs6427356 |
Map | rs6427356 |
PheGenI | rs6427356 |
Biobank | rs6427356 |
1000 genomes | rs6427356 |
hgdp | rs6427356 |
ensembl | rs6427356 |
geneview | rs6427356 |
scholar | rs6427356 |
rs6427356 | |
pharmgkb | rs6427356 |
gwascentral | rs6427356 |
openSNP | rs6427356 |
23andMe | rs6427356 |
SNPshot | rs6427356 |
SNPdbe | rs6427356 |
MSV3d | rs6427356 |
GWAS Ctlg | rs6427356 |
GMAF | 0.4793 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18951430] |
Trait | Attention-deficit/hyperactivity disorder and conduct disorder |
Title | Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
Risk Allele | G |
P-val | 0.000008 |
Odds Ratio | NR NR |