rs17110690
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17110690(A;A) |
Make rs17110690(A;G) |
Make rs17110690(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 72014217 |
Gene | TPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs17110690 |
dbSNP (classic) | rs17110690 |
ClinGen | rs17110690 |
ebi | rs17110690 |
HLI | rs17110690 |
Exac | rs17110690 |
Gnomad | rs17110690 |
Varsome | rs17110690 |
LitVar | rs17110690 |
Map | rs17110690 |
PheGenI | rs17110690 |
Biobank | rs17110690 |
1000 genomes | rs17110690 |
hgdp | rs17110690 |
ensembl | rs17110690 |
geneview | rs17110690 |
scholar | rs17110690 |
rs17110690 | |
pharmgkb | rs17110690 |
gwascentral | rs17110690 |
openSNP | rs17110690 |
23andMe | rs17110690 |
SNPshot | rs17110690 |
SNPdbe | rs17110690 |
MSV3d | rs17110690 |
GWAS Ctlg | rs17110690 |
GMAF | 0.2172 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25875332] Genome-Wide Analysis of Attention Deficit Hyperactivity Disorder in Norway