rs10153620
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10153620(C;C) |
Make rs10153620(C;G) |
Make rs10153620(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 205195913 |
Gene | PARD3B |
is a | snp |
is | mentioned by |
dbSNP | rs10153620 |
dbSNP (classic) | rs10153620 |
ClinGen | rs10153620 |
ebi | rs10153620 |
HLI | rs10153620 |
Exac | rs10153620 |
Gnomad | rs10153620 |
Varsome | rs10153620 |
LitVar | rs10153620 |
Map | rs10153620 |
PheGenI | rs10153620 |
Biobank | rs10153620 |
1000 genomes | rs10153620 |
hgdp | rs10153620 |
ensembl | rs10153620 |
geneview | rs10153620 |
scholar | rs10153620 |
rs10153620 | |
pharmgkb | rs10153620 |
gwascentral | rs10153620 |
openSNP | rs10153620 |
23andMe | rs10153620 |
SNPshot | rs10153620 |
SNPdbe | rs10153620 |
MSV3d | rs10153620 |
GWAS Ctlg | rs10153620 |
GMAF | 0.2727 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23527680] |
Trait | Attention deficit hyperactivity disorder (combined symptoms) |
Title | Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. |
Risk Allele | C |
P-val | 6E-6 |
Odds Ratio | NR NR |