present in Gene: LACC1
present in Chromosome: 13
Position on Chromosome: 43883789
Alleles of this Variant: A/G
rs3764147 in
LACC1 gene and
Asthma
PMID 21150878 2011 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.
rs3764147 in
LACC1 gene and
Crohn Disease
PMID 28067908 2017 Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
PMID 18587394 2008 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
PMID 21102463 2010 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.
PMID 23128233 2012 Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
rs3764147 in
LACC1 gene and
Inflammatory Bowel Diseases
PMID 26192919 2015 Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
PMID 28067908 2017 Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
rs3764147 in
LACC1 gene and
Leprosy
PMID 20018961 2009 Genomewide association study of leprosy.
PMID 22019778 2011 Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy.
rs3764147 in
LACC1 gene and
Multiple Sclerosis
PMID 22190364 2011 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.