Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE These findings suggest that C3435T is unlikely to be a marker for epilepsy multidrug resistance. 17460550 2007
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE For a single gene test, it was demonstrated that 3435C>T in the ABCB1 gene had a significant effect on epilepsy treatment responses, but polymorphisms in the NR1I2 gene did not. 17924830 2007
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE ABCB1 3435C>T was genotyped in 746 Han Chinese patients with epilepsy and 179 controls. 17521963 2007
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE The ABCB1 T-129C, C1236T, G2677T/A and C3435T polymorphisms were genotyped in 210 Japanese epileptics who had been prescribed AEDs, including CBZ, for longer than 2 years. 16753003 2006
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE One hundred and eight patients with drug-responsive epilepsy, 63 patients with drug-resistant epilepsy, and 219 control migraine subjects were studied, but the analysis for C3435T allele showed no significant association between the CC genotype and the multidrug-resistant epilepsy. 16542858 2006
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE The ABCB1 3435C-->T single-nucleotide polymorphism (SNP) or a three-SNP haplotype containing 3435C-->T has been implicated in multidrug resistance in epilepsy in three retrospective case-control studies, but a further three have failed to replicate the association. 16857572 2006
dbSNP: rs1045642
rs1045642
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1
CUI: C0014544
Disease:
Epilepsy
0.100 GeneticVariation BEFREE Whether the C3435T polymorphism can act as a marker for the natural history of treated epilepsy remains to be determined. 15857428 2005