rs2687116
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2687116(G;G) |
Make rs2687116(G;T) |
Make rs2687116(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 7 |
Position | 99768320 |
Gene | CYP3A4 |
is a | snp |
is | mentioned by |
dbSNP | rs2687116 |
dbSNP (classic) | rs2687116 |
ClinGen | rs2687116 |
ebi | rs2687116 |
HLI | rs2687116 |
Exac | rs2687116 |
Gnomad | rs2687116 |
Varsome | rs2687116 |
LitVar | rs2687116 |
Map | rs2687116 |
PheGenI | rs2687116 |
Biobank | rs2687116 |
1000 genomes | rs2687116 |
hgdp | rs2687116 |
ensembl | rs2687116 |
geneview | rs2687116 |
scholar | rs2687116 |
rs2687116 | |
pharmgkb | rs2687116 |
gwascentral | rs2687116 |
openSNP | rs2687116 |
23andMe | rs2687116 |
SNPshot | rs2687116 |
SNPdbe | rs2687116 |
MSV3d | rs2687116 |
GWAS Ctlg | rs2687116 |
Max Magnitude | 0 |
[PMID 28343093] Influence of genetic variants of CYP2D6, CYP2C9, CYP2C19 and CYP3A4 on antiepileptic drug metabolism in pediatric patients with refractory epilepsy.