rs1202199
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 |
Make rs1202199(C;T) |
Make rs1202199(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 20155943 |
Gene | MBOAT1 |
is a | snp |
is | mentioned by |
dbSNP | rs1202199 |
dbSNP (classic) | rs1202199 |
ClinGen | rs1202199 |
ebi | rs1202199 |
HLI | rs1202199 |
Exac | rs1202199 |
Gnomad | rs1202199 |
Varsome | rs1202199 |
LitVar | rs1202199 |
Map | rs1202199 |
PheGenI | rs1202199 |
Biobank | rs1202199 |
1000 genomes | rs1202199 |
hgdp | rs1202199 |
ensembl | rs1202199 |
geneview | rs1202199 |
scholar | rs1202199 |
rs1202199 | |
pharmgkb | rs1202199 |
gwascentral | rs1202199 |
openSNP | rs1202199 |
23andMe | rs1202199 |
SNPshot | rs1202199 |
SNPdbe | rs1202199 |
MSV3d | rs1202199 |
GWAS Ctlg | rs1202199 |
GMAF | 0.09963 |
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 | 0.000009 |
Odds Ratio | NR NR |