rs35191146
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(D;I) | Likely miscall by Ancestry | |
(G;G) | 0 | common/normal |
Make rs35191146(-;-) |
Make rs35191146(-;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 160139851 |
Gene | SLC22A1 |
is a | snp |
is | mentioned by |
dbSNP | rs35191146 |
dbSNP (classic) | rs35191146 |
ClinGen | rs35191146 |
ebi | rs35191146 |
HLI | rs35191146 |
Exac | rs35191146 |
Gnomad | rs35191146 |
Varsome | rs35191146 |
LitVar | rs35191146 |
Map | rs35191146 |
PheGenI | rs35191146 |
Biobank | rs35191146 |
1000 genomes | rs35191146 |
hgdp | rs35191146 |
ensembl | rs35191146 |
geneview | rs35191146 |
scholar | rs35191146 |
rs35191146 | |
pharmgkb | rs35191146 |
gwascentral | rs35191146 |
openSNP | rs35191146 |
23andMe | rs35191146 |
SNPshot | rs35191146 |
SNPdbe | rs35191146 |
MSV3d | rs35191146 |
GWAS Ctlg | rs35191146 |
Max Magnitude | 0 |
[PMID 23223357] The hOCT1 SNPs M420del and M408V alter imatinib uptake and M420del modifies clinical outcome in imatinib-treated chronic myeloid leukemia