rs4148737
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs4148737(A;A) |
Make rs4148737(A;G) |
Make rs4148737(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 87541836 |
Gene | ABCB1 |
is a | snp |
is | mentioned by |
dbSNP | rs4148737 |
dbSNP (classic) | rs4148737 |
ClinGen | rs4148737 |
ebi | rs4148737 |
HLI | rs4148737 |
Exac | rs4148737 |
Gnomad | rs4148737 |
Varsome | rs4148737 |
LitVar | rs4148737 |
Map | rs4148737 |
PheGenI | rs4148737 |
Biobank | rs4148737 |
1000 genomes | rs4148737 |
hgdp | rs4148737 |
ensembl | rs4148737 |
geneview | rs4148737 |
scholar | rs4148737 |
rs4148737 | |
pharmgkb | rs4148737 |
gwascentral | rs4148737 |
openSNP | rs4148737 |
23andMe | rs4148737 |
SNPshot | rs4148737 |
SNPdbe | rs4148737 |
MSV3d | rs4148737 |
GWAS Ctlg | rs4148737 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 27287205] Identification of genetic variants in pharmacokinetic genes associated with Ewing Sarcoma treatment outcome.