|
rs1003342
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
|
26192919 |
2015 |
|
rs1004819
|
|
|
0.020 |
GeneticVariation |
BEFREE |
IL23R is an IBD susceptibility gene, but has no epistatic interaction with CARD15 and SLC22A4/5. rs1004819 is the major IL23R variant associated with CD in the German population, while the p.Arg381Gln IL23R variant is a protective marker for CD and UC.
|
17786191 |
2007 |
|
rs1004819
|
|
|
0.020 |
GeneticVariation |
BEFREE |
This study was aimed to investigate the possible association of Crohn's disease (CD) with inflammatory bowel disease gene 5 (IBD5) IGR2198a_1 (rs11739135), IGR2096a_1 (rs12521868) and interleukin-23 receptor (IL23R) genetic variant (rs1004819) in the Malaysian population.
|
22908971 |
2012 |
|
rs10051722
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
|
26192919 |
2015 |
|
rs10061469
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
|
26192919 |
2015 |
|
rs10063949
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A genetic variant (rs10063949-G) in the SLC23A1 ascorbate transporter locus was identified and is associated with an increased risk of CD in a white Canadian IBD cohort.
|
24284447 |
2014 |
|
rs10065172
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Susceptibility to Crohn disease (CD), an inflammatory bowel disease, is influenced by common variants at many loci like the exonic synonymous IRGM SNP (rs10065172, NM_001145805.1, c.313C>T).
|
21508684 |
2011 |
|
rs10065637
|
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
|
26192919 |
2015 |
|
rs10114470
|
|
|
0.010 |
GeneticVariation |
BEFREE |
rs1250569 (ZMIZ1) and rs10114470 (TL1A) are two novel loci that indicate susceptibility to IBD in Han-Chinese patients.
|
28456797 |
2017 |
|
rs10142466
|
|
|
0.700 |
GeneticVariation |
GWASCAT |
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
|
26192919 |
2015 |
|
rs1020856343
|
|
|
0.020 |
GeneticVariation |
BEFREE |
To determine whether the TC haplotype is also associated with IBD in a Japanese population, we genotyped L503F and -207G/C variants in Japanese subjects.
|
16373276 |
2006 |
|
rs1020856343
|
|
|
0.020 |
GeneticVariation |
BEFREE |
The present results replicated the association of the OCTN1 rs1050152 (L503F) variant with CD and IBD overall.
|
21122496 |
2010 |
|
rs1042058
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
|
28067908 |
2017 |
|
rs1042058
|
|
C |
0.800 |
GeneticVariation |
GWASDB |
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
|
23128233 |
2012 |
|
rs1042058
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
|
23128233 |
2012 |
|
rs1042522
|
|
|
0.010 |
GeneticVariation |
BEFREE |
To investigate the associations between the rs1250569 (zinc finger MIZ-type containing 1, ZMIZ1), rs1042522 (tumour protein p53, TP53), and rs10114470 (tumour necrosis factor-like cytokine 1A, TL1A) polymorphisms and the development of inflammatory bowel disease (IBD) in a Chinese (Han) population.
|
28456797 |
2017 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The C3435T polymorphism of the ABCB1/MDR1 gene is not a risk factor for IBD, including UC and CD, in the population coming from central Poland.
|
22661185 |
2012 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
We carried out a case-control study to examine the association of MDR1 (C1236T and C3435T), GSTT1, and GSTM1 polymorphisms with the risk of IBD.
|
26604430 |
2015 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The role of the single nucleotide polymorphisms (SNPs) on positions 2677G>T/A and 3435C>T of the multi-drug-resistance gene 1 (MDR1) in inflammatory bowel disease (IBD) remains unclear.
|
17665184 |
2007 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
The statistically significant correlation was discovered between gender and C3435T</span> genotype both for IBD and CD patients, with 3435CT heterozygote prevailing in IBD and CD males.
|
25712653 |
2015 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Significant association of Ala893 with IBD was observed by both case-control analysis (P=.002) and the pedigree disequilibrium test (PDT [P=.00020-.00030]) but not for the Asn21Asp or C3435T polymorphisms.
|
14610718 |
2003 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
A meta-analysis was carried out of our results and those from 8 previously published association studies of the C3435T variant in inflammatory bowel disease.
|
16633048 |
2006 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
In this study we have undertaken a meta-analysis of the available findings obtained with two SNPs polymorphism (C3435T and G2677T/A) in IBD; a significant association of 3435T allele and 3435TT genotype has been found with UC (OR = 1.17, P = 0.003 and OR = 1.36, P = 0.017, respectively).
|
16773678 |
2006 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
Interestingly, a negative association was found between MDR1 C3435T polymorphism in patients with a positive family history for IBD (OR = 0.44; 95% CI: 0.20-0.95) and articular manifestations (OR = 0.29; 95% CI: 0.13-0.68).
|
17260353 |
2007 |
|
rs1045642
|
|
|
0.100 |
GeneticVariation |
BEFREE |
This meta-analysis indicated that the C3435T polymorphism of MDR1 may not confer susceptibility to IBD.
|
24449364 |
2014 |