Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1045642
rs1045642
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 GeneticVariation BEFREE Generally, indels rs34743033 and rs16430 were genotyped by PCR and polyacrylamide gel electrophoresis assay and SNPs rs2032582 and rs1045642 were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay in 110 Chinese AGC patients post-chemotherapy. 28074308

2017

dbSNP: rs1045642
rs1045642
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 GeneticVariation BEFREE This meta-analysis suggested that the MDR1 C3435T polymorphism is not associated with susceptibility to GC and PU. 24815441

2014

dbSNP: rs1045642
rs1045642
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 GeneticVariation BEFREE No correlation was observed between the C3435T polymorphism of the MDR1 gene and GC risk or prognosis in the population studied. 22641402

2012

dbSNP: rs1045642
rs1045642
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.040 GeneticVariation BEFREE In this preliminary data, the association with MDR1 C3435T polymorphism and risk for developing H. pylori-related gastric cancer and peptic ulcer in Japanese was low. 18644389

2008

dbSNP: rs2032582
rs2032582
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 GeneticVariation BEFREE To investigate the impacts of gene variations on survival outcomes of advanced gastric cancer (AGC) patients treated with 5‑fluorouracil (5-FU)-based chemotherapy, we analyzed the associations of 2 indels of the TS gene rs34743033 (double or triple tandem repeats of a 28 bp sequence in 5'-UTR, denoted as 2R or 3R allele) and rs16430 (a 6 bp variation at 1494 bp in 3'-UTR, denoted as ins6 or del6 allele) and 2 single nucleotide polymorphisms (SNPs) of ABCB1gene rs2032582 in exon 21 and rs1045642 in exon 26, with clinical outcomes after 5‑FU treatment. 28074308

2017