rs6733379
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6733379(G;G) |
Make rs6733379(G;T) |
Make rs6733379(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 34255008 |
Gene | LINC01317 |
is a | snp |
is | mentioned by |
dbSNP | rs6733379 |
dbSNP (classic) | rs6733379 |
ClinGen | rs6733379 |
ebi | rs6733379 |
HLI | rs6733379 |
Exac | rs6733379 |
Gnomad | rs6733379 |
Varsome | rs6733379 |
LitVar | rs6733379 |
Map | rs6733379 |
PheGenI | rs6733379 |
Biobank | rs6733379 |
1000 genomes | rs6733379 |
hgdp | rs6733379 |
ensembl | rs6733379 |
geneview | rs6733379 |
scholar | rs6733379 |
rs6733379 | |
pharmgkb | rs6733379 |
gwascentral | rs6733379 |
openSNP | rs6733379 |
23andMe | rs6733379 |
SNPshot | rs6733379 |
SNPdbe | rs6733379 |
MSV3d | rs6733379 |
GWAS Ctlg | rs6733379 |
GMAF | 0.2259 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 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 | 0.000004 |
Odds Ratio | NR NR |