rs10797919
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;G) | 0 | common in complete genomics |
Make rs10797919(C;C) |
Make rs10797919(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 183883780 |
Gene | RGL1 |
is a | snp |
is | mentioned by |
dbSNP | rs10797919 |
dbSNP (classic) | rs10797919 |
ClinGen | rs10797919 |
ebi | rs10797919 |
HLI | rs10797919 |
Exac | rs10797919 |
Gnomad | rs10797919 |
Varsome | rs10797919 |
LitVar | rs10797919 |
Map | rs10797919 |
PheGenI | rs10797919 |
Biobank | rs10797919 |
1000 genomes | rs10797919 |
hgdp | rs10797919 |
ensembl | rs10797919 |
geneview | rs10797919 |
scholar | rs10797919 |
rs10797919 | |
pharmgkb | rs10797919 |
gwascentral | rs10797919 |
openSNP | rs10797919 |
23andMe | rs10797919 |
SNPshot | rs10797919 |
SNPdbe | rs10797919 |
MSV3d | rs10797919 |
GWAS Ctlg | rs10797919 |
GMAF | 0.4454 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18951430] |
Trait | Attention-deficit/hyperactivity disorder and conduct disorder |
Title | Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
Risk Allele | G |
P-val | 0.000009 |
Odds Ratio | NR NR |