rs10895959
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10895959(A;A) |
Make rs10895959(A;G) |
Make rs10895959(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 106459435 |
is a | snp |
is | mentioned by |
dbSNP | rs10895959 |
dbSNP (classic) | rs10895959 |
ClinGen | rs10895959 |
ebi | rs10895959 |
HLI | rs10895959 |
Exac | rs10895959 |
Gnomad | rs10895959 |
Varsome | rs10895959 |
LitVar | rs10895959 |
Map | rs10895959 |
PheGenI | rs10895959 |
Biobank | rs10895959 |
1000 genomes | rs10895959 |
hgdp | rs10895959 |
ensembl | rs10895959 |
geneview | rs10895959 |
scholar | rs10895959 |
rs10895959 | |
pharmgkb | rs10895959 |
gwascentral | rs10895959 |
openSNP | rs10895959 |
23andMe | rs10895959 |
SNPshot | rs10895959 |
SNPdbe | rs10895959 |
MSV3d | rs10895959 |
GWAS Ctlg | rs10895959 |
GMAF | 0.3737 |
Max Magnitude | 0 |
? | (A;A) (A;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 |