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SNP information rs10210302

RS10210302

Normal allele: CC

Polymorphism rs10210302 is related to topics like this:

Crohn's disease genetic

A chronic disorder known as Crohn's disease is a multi-faceted condition that primarily impacts the...


Research and publications:

  18224312   Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment

  18438406   Genetic determinants of ulcerative colitis include the ECM1 locus and five loci involved in Crohn's disease.

  18533027   Worldwide population differentiation at disease-associated SNPs

  20846217   Association of linear growth impairment in pediatric Crohn's disease and known growth locus: a pilot study.

  21217814   Presymptomatic risk assessment for chronic non-communicable diseases.

  21548950   Evaluation of 22 genetic variants with risk for Crohn's disease in an Ashkenazi Jewish population: a case-control study.

  21618365   Distortion of transmission of the Crohn's disease risk gene ATG16L1 leads to sex differences in disease association.

  25712183   Genetic polymorphism of the ATG16L1 gene influences the response to adalimumab in patients with Crohn's disease.

  26833331   Retrospective Binary-Trait Association Test Elucidates Genetic Architecture of Crohn Disease.

  26861312   Association between Genetic Polymorphisms and Response to Anti-TNFs in Patients with Inflammatory Bowel Disease.

  27153677   Assessing statistical significance in multivariable genome wide association analysis.

  27366220   Predicting durable response or resistance to antitumor necrosis factor therapy in inflammatory bowel disease.

  27417569   Systematic review: genetic biomarkers associated with anti-TNF treatment response in inflammatory bowel diseases.

  27892471   Combining Multiple Hypothesis Testing with Machine Learning Increases the Statistical Power of Genome-wide Association Studies.

  28542425   Association of ATG16L1 gene haplotype with inflammatory bowel disease in Indians.

  28603427   Pharmacogenetics in inflammatory bowel disease: understanding treatment response and personalizing therapeutic strategies.

  29228965   Genetic polymorphism in ATG16L1 gene is associated with adalimumab use in inflammatory bowel disease.

  33147747   Pathogenic Single Nucleotide Polymorphisms on Autophagy-Related Genes.

  34208077   Association of ATG16L1 variations with clinical phenotypes of Still's disease in adults.

Is rheumatoid arthritis genetic

Chronic abnormal inflammation is the hallmark of rheumatoid arthritis, a disease that primarily...

Hereditary pancreatitis

Pancreatitis is a multifaceted ailment that can stem from various sources. If pancreatitis arises...

Heart attack genetic

Genetic predisposition, also referred to as familial predisposition, is a crucial risk factor for...

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