rs272000
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs272000(C;C) |
Make rs272000(C;G) |
Make rs272000(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 115898219 |
is a | snp |
is | mentioned by |
dbSNP | rs272000 |
dbSNP (classic) | rs272000 |
ClinGen | rs272000 |
ebi | rs272000 |
HLI | rs272000 |
Exac | rs272000 |
Gnomad | rs272000 |
Varsome | rs272000 |
LitVar | rs272000 |
Map | rs272000 |
PheGenI | rs272000 |
Biobank | rs272000 |
1000 genomes | rs272000 |
hgdp | rs272000 |
ensembl | rs272000 |
geneview | rs272000 |
scholar | rs272000 |
rs272000 | |
pharmgkb | rs272000 |
gwascentral | rs272000 |
openSNP | rs272000 |
23andMe | rs272000 |
SNPshot | rs272000 |
SNPdbe | rs272000 |
MSV3d | rs272000 |
GWAS Ctlg | rs272000 |
GMAF | 0.4366 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18821565] |
Trait | Attention deficit hyperactivity disorder |
Title | Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations |
Risk Allele | |
P-val | 0.000009 |
Odds Ratio | NR NR |
[PMID 20145962] Molecular genetics of attention-deficit/hyperactivity disorder: an overview.
[PMID 20148275] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.