rs10487524
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs10487524(C;C) |
Make rs10487524(C;T) |
Make rs10487524(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 145144438 |
Gene | LOC105375551 |
is a | snp |
is | mentioned by |
dbSNP | rs10487524 |
dbSNP (classic) | rs10487524 |
ClinGen | rs10487524 |
ebi | rs10487524 |
HLI | rs10487524 |
Exac | rs10487524 |
Gnomad | rs10487524 |
Varsome | rs10487524 |
LitVar | rs10487524 |
Map | rs10487524 |
PheGenI | rs10487524 |
Biobank | rs10487524 |
1000 genomes | rs10487524 |
hgdp | rs10487524 |
ensembl | rs10487524 |
geneview | rs10487524 |
scholar | rs10487524 |
rs10487524 | |
pharmgkb | rs10487524 |
gwascentral | rs10487524 |
openSNP | rs10487524 |
23andMe | rs10487524 |
SNPshot | rs10487524 |
SNPdbe | rs10487524 |
MSV3d | rs10487524 |
GWAS Ctlg | rs10487524 |
GMAF | 0.2277 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20732626![]() |
Trait | |
Title | Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder |
Risk Allele | T |
P-val | 0.000009 |
Odds Ratio | 1.60 [NR] |