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SNP information rs6498169

RS6498169

Normal allele: AA

CLEC16A variant, is associated with autoimmune diseases, particularly multiple sclerosis and type I diabetes.

Polymorphism rs6498169 is related to topics like this:

Is multiple sclerosis hereditary disease

The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...


Research and publications:

  18650830   Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians.

  18987646   The expanding genetic overlap between multiple sclerosis and type I diabetes.

  19221398   Chromosomal region 16p13: further evidence of increased predisposition to immune diseases.

  19317741   Autoimmune disease association signals in CIITA and KIAA0350 are not involved in celiac disease susceptibility.

  19337309   Specific association of the CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) patients with Crohn's disease.

  19734133   A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis.

  19865102   Multiple sclerosis susceptibility alleles in African Americans.

  20007504   Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci.

  20211854   CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.

  20220768   A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis.

  20362272   Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come.

  20368992   Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.

  21179112   Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus.

  21247752   Revealing the genetic basis of multiple sclerosis: are we there yet?

  22492128   Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease.

  23133532   Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women.

  23251581   Meta-analysis of 125 rheumatoid arthritis-related single nucleotide polymorphisms studied in the past two decades.

  24646814   Polymorphisms of CLEC16A region and autoimmune thyroid diseases.

  25576669   The CLEC16A gene variant provides protection against Vogt-Koyanagi-Harada syndrome but not Behçet's disease in the Chinese Han population.

  28617357   [Polymorphic variants of the immune response genes as risk factors for primary progressive multiple sclerosis].

  30711878   Genetic differences between primary progressive and relapsing-remitting multiple sclerosis: The impact of immune-related genes variability.

  31482761   Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

  35432448   CLEC16A variants associated with autoimmune diseases confer risk for Parkinson's disease in Han Chinese.

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