rs1644305
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1644305(C;C) |
Make rs1644305(C;T) |
Make rs1644305(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 133867905 |
is a | snp |
is | mentioned by |
dbSNP | rs1644305 |
dbSNP (classic) | rs1644305 |
ClinGen | rs1644305 |
ebi | rs1644305 |
HLI | rs1644305 |
Exac | rs1644305 |
Gnomad | rs1644305 |
Varsome | rs1644305 |
LitVar | rs1644305 |
Map | rs1644305 |
PheGenI | rs1644305 |
Biobank | rs1644305 |
1000 genomes | rs1644305 |
hgdp | rs1644305 |
ensembl | rs1644305 |
geneview | rs1644305 |
scholar | rs1644305 |
rs1644305 | |
pharmgkb | rs1644305 |
gwascentral | rs1644305 |
openSNP | rs1644305 |
23andMe | rs1644305 |
SNPshot | rs1644305 |
SNPdbe | rs1644305 |
MSV3d | rs1644305 |
GWAS Ctlg | rs1644305 |
GMAF | 0.3053 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | A |
P-val | 0.000008 |
Odds Ratio | NR NR |