rs2769967
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2769967(C;C) |
Make rs2769967(C;G) |
Make rs2769967(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 79274443 |
is a | snp |
is | mentioned by |
dbSNP | rs2769967 |
dbSNP (classic) | rs2769967 |
ClinGen | rs2769967 |
ebi | rs2769967 |
HLI | rs2769967 |
Exac | rs2769967 |
Gnomad | rs2769967 |
Varsome | rs2769967 |
LitVar | rs2769967 |
Map | rs2769967 |
PheGenI | rs2769967 |
Biobank | rs2769967 |
1000 genomes | rs2769967 |
hgdp | rs2769967 |
ensembl | rs2769967 |
geneview | rs2769967 |
scholar | rs2769967 |
rs2769967 | |
pharmgkb | rs2769967 |
gwascentral | rs2769967 |
openSNP | rs2769967 |
23andMe | rs2769967 |
SNPshot | rs2769967 |
SNPdbe | rs2769967 |
MSV3d | rs2769967 |
GWAS Ctlg | rs2769967 |
GMAF | 0.4977 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18821565] |
Trait | Inattentive symptoms |
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 | 0.000003 |
Odds Ratio | NR NR |