rs701157
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs701157(C;C) |
Make rs701157(C;T) |
Make rs701157(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 230539080 |
is a | snp |
is | mentioned by |
dbSNP | rs701157 |
dbSNP (classic) | rs701157 |
ClinGen | rs701157 |
ebi | rs701157 |
HLI | rs701157 |
Exac | rs701157 |
Gnomad | rs701157 |
Varsome | rs701157 |
LitVar | rs701157 |
Map | rs701157 |
PheGenI | rs701157 |
Biobank | rs701157 |
1000 genomes | rs701157 |
hgdp | rs701157 |
ensembl | rs701157 |
geneview | rs701157 |
scholar | rs701157 |
rs701157 | |
pharmgkb | rs701157 |
gwascentral | rs701157 |
openSNP | rs701157 |
23andMe | rs701157 |
SNPshot | rs701157 |
SNPdbe | rs701157 |
MSV3d | rs701157 |
GWAS Ctlg | rs701157 |
GMAF | 0.4642 |
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 | C |
P-val | 0.000004 |
Odds Ratio | NR NR |