rs2239393
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2239393(A;A) |
Make rs2239393(A;G) |
Make rs2239393(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 19962905 |
Gene | COMT, MIR4761 |
is a | snp |
is | mentioned by |
dbSNP | rs2239393 |
dbSNP (classic) | rs2239393 |
ClinGen | rs2239393 |
ebi | rs2239393 |
HLI | rs2239393 |
Exac | rs2239393 |
Gnomad | rs2239393 |
Varsome | rs2239393 |
LitVar | rs2239393 |
Map | rs2239393 |
PheGenI | rs2239393 |
Biobank | rs2239393 |
1000 genomes | rs2239393 |
hgdp | rs2239393 |
ensembl | rs2239393 |
geneview | rs2239393 |
scholar | rs2239393 |
rs2239393 | |
pharmgkb | rs2239393 |
gwascentral | rs2239393 |
openSNP | rs2239393 |
23andMe | rs2239393 |
SNPshot | rs2239393 |
SNPdbe | rs2239393 |
MSV3d | rs2239393 |
GWAS Ctlg | rs2239393 |
GMAF | 0.3811 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21206424] Novel Polymorphisms Associated With Tacrolimus Trough Concentrations: Results From a Multicenter Kidney Transplant Consortium
[PMID 18937309] Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.
[PMID 19094200] Genetic variation in the catechol-O-methyltransferase (COMT) gene and morphine requirements in cancer patients with pain.