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SNP information rs7775228

RS7775228

Normal allele: TT

HLA DQ2.2 genes play an important role in many autoimmune diseases such as celiac disease, type 1 diabetes, rheumatoid arthritis, multiple sclerosis, psoriasis and others.

Polymorphism rs7775228 is related to topics like this:

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Research and publications:

  18509540   Effective detection of human leukocyte antigen risk alleles in celiac disease using tag single nucleotide polymorphisms.

  19458352   Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.

  19950296   Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1.

  20305777   New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study.

  20398668   Detection of celiac disease and lymphocytic enteropathy by parallel serology and histopathology in a population-based study.

  21853121   Large scale replication study of the association between HLA class II/BTNL2 variants and osteoarthritis of the knee in European-descent populations.

  22006220   Integrating pathway analysis and genetics of gene expression for genome-wide association study of basal cell carcinoma.

  22036096   A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.

  23755072   Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma.

  23868913   Advances in osteoarthritis genetics.

  24876751   Allele and haplotype frequencies for HLA-DQ in Iranian celiac disease patients.

  25749780   Association of Single Nucleotide Polymorphisms in the MD-2 Gene Promoter Region With Der p 2 Allergy.

  26214689   Genetic Loci Associated with Allergic Sensitization in Lithuanians.

  27449795   Shared and unique common genetic determinants between pediatric and adult celiac disease.

  27764105   Genome-Wide Meta-Analysis of Sciatica in Finnish Population.

  28056976   A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients.

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

  31605414   Association of GWAS-supported noncoding area loci rs404860, rs3117098, and rs7775228 with asthma in Chinese Zhuang population.

  32082391   Replication study of susceptibility variants associated with allergic rhinitis and allergy in Han Chinese.

  33170161   Genetic test for the prescription of diets in support of physical activity.

  33217039   Two tagging single-nucleotide polymorphisms to capture HLA-DRB1*07:01-DQA1*02:01-DQB1*02:02 haplotype associated with asparaginase hypersensitivity.

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