rs1471225
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1471225(C;C) |
Make rs1471225(C;T) |
Make rs1471225(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 29596192 |
is a | snp |
is | mentioned by |
dbSNP | rs1471225 |
dbSNP (classic) | rs1471225 |
ClinGen | rs1471225 |
ebi | rs1471225 |
HLI | rs1471225 |
Exac | rs1471225 |
Gnomad | rs1471225 |
Varsome | rs1471225 |
LitVar | rs1471225 |
Map | rs1471225 |
PheGenI | rs1471225 |
Biobank | rs1471225 |
1000 genomes | rs1471225 |
hgdp | rs1471225 |
ensembl | rs1471225 |
geneview | rs1471225 |
scholar | rs1471225 |
rs1471225 | |
pharmgkb | rs1471225 |
gwascentral | rs1471225 |
openSNP | rs1471225 |
23andMe | rs1471225 |
SNPshot | rs1471225 |
SNPdbe | rs1471225 |
MSV3d | rs1471225 |
GWAS Ctlg | rs1471225 |
GMAF | 0.4201 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | 0.000008 |
Odds Ratio | NR NR |
[PMID 20148275] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.