rs717620
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs717620(A;A) |
Make rs717620(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 99782821 |
Gene | ABCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs717620 |
dbSNP (classic) | rs717620 |
ClinGen | rs717620 |
ebi | rs717620 |
HLI | rs717620 |
Exac | rs717620 |
Gnomad | rs717620 |
Varsome | rs717620 |
LitVar | rs717620 |
Map | rs717620 |
PheGenI | rs717620 |
Biobank | rs717620 |
1000 genomes | rs717620 |
hgdp | rs717620 |
ensembl | rs717620 |
geneview | rs717620 |
scholar | rs717620 |
rs717620 | |
pharmgkb | rs717620 |
gwascentral | rs717620 |
openSNP | rs717620 |
23andMe | rs717620 |
SNPshot | rs717620 |
SNPdbe | rs717620 |
MSV3d | rs717620 |
GWAS Ctlg | rs717620 |
GMAF | 0.1763 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 21451505] Effect of ABCC2 (MRP2) Transport Function on Erythromycin Metabolism
[PMID 22630058] ABCC2 Polymorphisms and Haplotype are Associated with Drug Resistance in Chinese Epileptic Patients
[PMID 17997497] Association of the multidrug-resistance-associated protein gene (ABCC2) variants with intrahepatic cholestasis of pregnancy.
[PMID 18926681] Polymorphisms of MRP2 (ABCC2) are associated with susceptibility to nonalcoholic fatty liver disease.
[PMID 19568750] MRP2 and GSTP1 polymorphisms and chemotherapy response in advanced non-small cell lung cancer.
[PMID 20061166] Genetic polymorphisms influence mycophenolate mofetil-related adverse events in pediatric heart transplant patients.
[PMID 20139798] ADME pharmacogenetics: investigation of the pharmacokinetics of the antiretroviral agent lopinavir coformulated with ritonavir.
[PMID 22318656] Interindividual variability in hepatic expression of the multidrug resistance-associated protein 2 (MRP2/ABCC2): quantification by liquid chromatography/tandem mass spectrometry.
[PMID 22473764] A comprehensive study of polymorphisms in ABCB1, ABCC2 and ABCG2 and lung cancer chemotherapy response and prognosis.
[PMID 23506516] A systematic review and meta-analysis of the role of ABCC2 variants on drug response in patients with epilepsy
[PMID 22868256] A prospective validation pharmacogenomic study in the adjuvant setting of colorectal cancer patients treated with the 5-fluorouracil/leucovorin/oxaliplatin (FOLFOX4) regimen.
[PMID 23069858] Impact of ABCC2 polymorphisms on high-dose methotrexate pharmacokinetics in patients with lymphoid malignancy.
[PMID 24782687] Multi-institutional Study of Outcomes After Pediatric Heart Transplantation: Candidate Gene Polymorphism Analysis of ABCC2
[PMID 25007187] Genetic polymorphisms in candidate genes predict increased toxicity with methotrexate therapy in Lebanese children with acute lymphoblastic leukemia
[PMID 26107220] Quantitative Assessment of the Association between ABC Polymorphisms and Osteosarcoma Response: a Meta-analysis
[PMID 26189305] ABCB1, ABCC2, SCN1A, SCN2A, GABRA1 gene polymorphisms and drug resistant epilepsy in the Chinese Han population
[PMID 26807589] A Single-Nucleotide Polymorphism in ABCC4 Is Associated with Tenofovir-Related Beta2-Microglobulinuria in Thai Patients with HIV-1 Infection.
[PMID 27566582] Pharmacogenetic analysis of high-dose methotrexate treatment in children with osteosarcoma.
ClinVar | |
---|---|
Risk | rs717620(A;A) |
Alt | rs717620(A;A) |
Reference | Rs717620(G;G) |
Significance | Probable-non-pathogenic |
Disease | Dubin-Johnson syndrome |
Variation | info |
Gene | ABCC2 |
CLNDBN | Dubin-Johnson syndrome |
Reversed | 1 |
HGVS | NC_000010.10:g.101542578C>T |
CLNSRC | |
CLNACC | RCV000404794.1, |
[PMID 30024814] Association of ABCC2 polymorphism and gender with high-density lipoprotein cholesterol response to simvastatin.
[PMID 31391850] Role of Four ABC Transporter Genes in Pharmacogenetic Susceptibility to Breast Cancer in Jordanian Patients.
- Is a snp
- In dbSNP
- SNPs on chromosome 10
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip 23andMe v5
- On chip Affy GenomeWide 6
- On chip Ancestry v2c
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip Ancestry v2d