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rs2289669

From SNPedia

Orientationplus
Stabilizedplus
Make rs2289669(A;A)
Make rs2289669(A;G)
Make rs2289669(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position19560030
GeneSLC47A1
is asnp
is mentioned by
dbSNPrs2289669
ebirs2289669
HLIrs2289669
Exacrs2289669
Varsomers2289669
Maprs2289669
PheGenIrs2289669
hapmaprs2289669
1000 genomesrs2289669
hgdprs2289669
ensemblrs2289669
gopubmedrs2289669
geneviewrs2289669
scholarrs2289669
googlers2289669
pharmgkbrs2289669
gwascentralrs2289669
openSNPrs2289669
23andMers2289669
23andMe allrs2289669
SNP Nexus

SNPshotrs2289669
SNPdbers2289669
MSV3drs2289669
GWAS Ctlgrs2289669
GMAF0.343
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 19898263] Interaction between polymorphisms in the OCT1 and MATE1 transporter and metformin response


[PMID 21241070] Clinical pharmacokinetics of metformin


[PMID 19074986OA-icon.png] Expansion of human regulatory T-cells from patients with type 1 diabetes.


[PMID 19228809OA-icon.png] Genetic variation in the multidrug and toxin extrusion 1 transporter protein influences the glucose-lowering effect of metformin in patients with diabetes: a preliminary study.


[PMID 22569819] Effects of genetic variants in SLC22A2 organic cation transporter 2 and SLC47A1 multidrug and toxin extrusion 1 transporter on cisplatin-induced adverse events.


[PMID 22882994] Pharmacogenomic association between a variant in SLC47A1 gene and therapeutic response to metformin in type 2 diabetes.


[PMID 26004431] SLC47A1 gene rs2289669 G>A variants enhance the glucose-lowering effect of metformin via delaying its excretion in Chinese type 2 diabetes patients