rs864643
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs864643(C;C) |
Make rs864643(C;T) |
Make rs864643(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 39514089 |
Gene | MOBP |
is a | snp |
is | mentioned by |
dbSNP | rs864643 |
dbSNP (classic) | rs864643 |
ClinGen | rs864643 |
ebi | rs864643 |
HLI | rs864643 |
Exac | rs864643 |
Gnomad | rs864643 |
Varsome | rs864643 |
LitVar | rs864643 |
Map | rs864643 |
PheGenI | rs864643 |
Biobank | rs864643 |
1000 genomes | rs864643 |
hgdp | rs864643 |
ensembl | rs864643 |
geneview | rs864643 |
scholar | rs864643 |
rs864643 | |
pharmgkb | rs864643 |
gwascentral | rs864643 |
openSNP | rs864643 |
23andMe | rs864643 |
SNPshot | rs864643 |
SNPdbe | rs864643 |
MSV3d | rs864643 |
GWAS Ctlg | rs864643 |
GMAF | 0.3085 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18839057] |
Trait | Attention-deficit/hyperactivity disorder |
Title | Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies |
Risk Allele | |
P-val | 1E-8 |
Odds Ratio | NR NR |
[PMID 17357082] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.