PMID 25936594 2015 Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.
rs886424 in
LINC00243 gene and
Lupus Erythematosus, Systemic
PMID 24871463 2014 GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.
rs886424 in
LINC00243 gene and
Malignant neoplasm of lung
PMID 22899653 2012 Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.
rs886424 in
LINC00243 gene and
Mental disorders
PMID 22688191 2012 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
rs886424 in
LINC00243 gene and
Myasthenia Gravis
PMID 23055271 2012 Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.
rs886424 in
LINC00243 gene and
Psychotic Disorders
PMID 22688191 2012 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
rs886424 in
LINC00243 gene and
Schizophrenia
PMID 22688191 2012 No single-nucleotide polymorphisms (SNPs) achieved significance in these new samples; however, combining new and previously reported SCZ samples (2111 SCZ and 2535 controls) revealed a genome-wide significant association in the major histocompatibility complex (MHC) region (rs886424, P=4.54 × 10(-8)).