rs41441749
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs41441749(C;C) |
Make rs41441749(C;T) |
Make rs41441749(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 18791492 |
is a | snp |
is | mentioned by |
dbSNP | rs41441749 |
dbSNP (classic) | rs41441749 |
ClinGen | rs41441749 |
ebi | rs41441749 |
HLI | rs41441749 |
Exac | rs41441749 |
Gnomad | rs41441749 |
Varsome | rs41441749 |
LitVar | rs41441749 |
Map | rs41441749 |
PheGenI | rs41441749 |
Biobank | rs41441749 |
1000 genomes | rs41441749 |
hgdp | rs41441749 |
ensembl | rs41441749 |
geneview | rs41441749 |
scholar | rs41441749 |
rs41441749 | |
pharmgkb | rs41441749 |
gwascentral | rs41441749 |
openSNP | rs41441749 |
23andMe | rs41441749 |
SNPshot | rs41441749 |
SNPdbe | rs41441749 |
MSV3d | rs41441749 |
GWAS Ctlg | rs41441749 |
GMAF | 0.1722 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18821565] |
Trait | Hyperactive-impulsive 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 | 0.000001 |
Odds Ratio | NR NR |