Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11175593
rs11175593
LRRK2 ; LINC02471 ; LOC105369735 ; LRRK2-DT
0.820 GeneticVariation BEFREE CD susceptibility polymorphisms ATG16L1 rs2241880, ICAM1 rs5498, IL4 rs2070874, IL17F rs763780, IRGM rs13361189, ITLN1 rs2274910, LRRK2 rs11175593, and TLR4 rs4986790 were genotyped in a Portuguese population (511 CD patients, 626 controls) and assessed for association with CD clinical characteristics. 22573572

2013
dbSNP: rs11175593
rs11175593
LRRK2 ; LINC02471 ; LOC105369735 ; LRRK2-DT
0.820 GeneticVariation BEFREE Genome-wide association studies (GWAS) in Crohn's disease (CD) have identified associations with single-nucleotide polymorphism (SNP) rs11175593 at chromosome 12q12. 23619718

2013
dbSNP: rs11175593
rs11175593
LRRK2 ; LINC02471 ; LOC105369735 ; LRRK2-DT
T 0.820 GeneticVariation GWASCAT Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008
dbSNP: rs11175593
rs11175593
LRRK2 ; LINC02471 ; LOC105369735 ; LRRK2-DT
T 0.820 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008