rs17228156
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17228156(C;C) |
Make rs17228156(C;T) |
Make rs17228156(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 81207084 |
Gene | RASGRF2 |
is a | snp |
is | mentioned by |
dbSNP | rs17228156 |
dbSNP (classic) | rs17228156 |
ClinGen | rs17228156 |
ebi | rs17228156 |
HLI | rs17228156 |
Exac | rs17228156 |
Gnomad | rs17228156 |
Varsome | rs17228156 |
LitVar | rs17228156 |
Map | rs17228156 |
PheGenI | rs17228156 |
Biobank | rs17228156 |
1000 genomes | rs17228156 |
hgdp | rs17228156 |
ensembl | rs17228156 |
geneview | rs17228156 |
scholar | rs17228156 |
rs17228156 | |
pharmgkb | rs17228156 |
gwascentral | rs17228156 |
openSNP | rs17228156 |
23andMe | rs17228156 |
SNPshot | rs17228156 |
SNPdbe | rs17228156 |
MSV3d | rs17228156 |
GWAS Ctlg | rs17228156 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21130132] |
Trait | Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) |
Title | Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder. |
Risk Allele | C |
P-val | 8E-6 |
Odds Ratio | NR NR |