Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1050152
rs1050152
0.040 GeneticVariation BEFREE Other studies have found that mutation of rs1143627 of IL1B (allelic model: OR 2.97; 95% CI 1.74-5.05, P < 0.001) and rs1050152 of OCTN1 (allelic model: OR 1.637, 95% CI 1.078-2.485, P = 0.021) increased the proportion of IBD-associated CRC in the population. 28243990

2017

dbSNP: rs1050152
rs1050152
0.040 GeneticVariation BEFREE To understand how turmeric may influence the consequences of a genetic predisposition to inappropriate inflammation, we used HEK293 cells to examine the in vitro capacity of turmeric extract and fractions to affect the functionality of two gene variants, solute carrier protein 22 A4 (SLC22A4, rs1050152) and interleukin-10 (IL-10, rs1800896) associated with IBD. 25314644

2014

dbSNP: rs1050152
rs1050152
0.040 GeneticVariation BEFREE The present results replicated the association of the OCTN1 rs1050152 (L503F) variant with CD and IBD overall. 21122496

2010

dbSNP: rs1050152
rs1050152
0.040 GeneticVariation BEFREE The present results replicated the association of the OCTN1 rs1050152 (L503F) variant with CD and IBD overall. 21122496

2010

dbSNP: rs1050152
rs1050152
0.040 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