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SNP information rs6903608

RS6903608

Normal allele: TT

Polymorphism rs6903608 is related to topics like this:

Leukemia is it genetic

Acute myeloid leukemia (AML) is a diverse cancer that primarily impacts individuals aged 60 and...

Research and publications:

  19122664   Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.

  20018015   Elastic-net regularization approaches for genome-wide association studies of rheumatoid arthritis.

  20018075   Genome-wide association study of rheumatoid arthritis by a score test based on wavelet transformation.

  20018081   Assessment of gene-covariate interactions by incorporating covariates into association mapping.

  20176734   Comparative genetic analysis of inflammatory bowel disease and type 1 diabetes implicates multiple loci with opposite effects.

  21037568   A genome-wide association study of Hodgkin lymphoma identified novel susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).

  22086417   A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32.

  22253788   Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations.

  22286212   Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.

  23326239   A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).

  23955597   Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.

  24151499   New insights into the genetic mechanism of IQ in autism spectrum disorders.

  24367763   Human leukocyte antigens and epstein-barr virus-associated nasopharyngeal carcinoma: old associations offer new clues into the role of immunity in infection-associated cancers.

  24727690   Single nucleotide polymorphism (SNP)-strings: an alternative method for assessing genetic associations.

  25648508   Modeling HLA associations with EBV-positive and -negative Hodgkin lymphoma suggests distinct mechanisms in disease pathogenesis.

  26019233   Dissecting the genetics of the human transcriptome identifies novel trait-related trans-eQTLs and corroborates the regulatory relevance of non-protein coding loci†.

  26405224   Familial predisposition and genetic risk factors for lymphoma.

  27600067   SNP Array in Hematopoietic Neoplasms: A Review.

  30154825   To ERV Is Human: A Phenotype-Wide Scan Linking Polymorphic Human Endogenous Retrovirus-K Insertions to Complex Phenotypes.

  33096882   The HLA Variant rs6903608 Is Associated with Disease Onset and Relapse of Immune-Mediated Thrombotic Thrombocytopenic Purpura in Caucasians.

  34687232   Next-generation sequencing and genotype association studies reveal the association of HLA-DRB3*02:02 with delayed hypersensitivity to penicillins.

Is drug abuse genetic

There is a significant interest among individuals, particularly those with a familial background of...

Obesity genes

Although physical inactivity and consuming energy-dense foods are commonly identified as the main...

Psoriasis is a genetic disease

It is beneficial to comprehend the genetic impact on the molecular mechanisms and pathways that...

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