rs4810685
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4810685(C;C) |
Make rs4810685(C;T) |
Make rs4810685(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 47771969 |
Gene | SULF2 |
is a | snp |
is | mentioned by |
dbSNP | rs4810685 |
dbSNP (classic) | rs4810685 |
ClinGen | rs4810685 |
ebi | rs4810685 |
HLI | rs4810685 |
Exac | rs4810685 |
Gnomad | rs4810685 |
Varsome | rs4810685 |
LitVar | rs4810685 |
Map | rs4810685 |
PheGenI | rs4810685 |
Biobank | rs4810685 |
1000 genomes | rs4810685 |
hgdp | rs4810685 |
ensembl | rs4810685 |
geneview | rs4810685 |
scholar | rs4810685 |
rs4810685 | |
pharmgkb | rs4810685 |
gwascentral | rs4810685 |
openSNP | rs4810685 |
23andMe | rs4810685 |
SNPshot | rs4810685 |
SNPdbe | rs4810685 |
MSV3d | rs4810685 |
GWAS Ctlg | rs4810685 |
GMAF | 0.3678 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18937294![]() |
Trait | Attention deficit hyperactivity disorder (time to onset) |
Title | Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder |
Risk Allele | C |
P-val | 0.000007 |
Odds Ratio | NR NR |
[PMID 20148275] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.