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SNP information rs1805081

Normal allele: CC

Polymorphism rs1805081 is related to topics like this:

Obesity genes

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


Research and publications:

  18834923   Variation in NPC1, the gene encoding Niemann-Pick C1, a protein involved in intracellular cholesterol transport, is associated with Alzheimer disease and/or aging in the Polish population.

  19553259   Common body mass index-associated variants confer risk of extreme obesity

  20110568   Combined analyses of 20 common obesity susceptibility variants.

  20127379   From monogenic to polygenic obesity: recent advances.

  20616199   Evaluation of genetic susceptibility loci for obesity in Chinese women.

  20712903   Obesity and diabetes genes are associated with being born small for gestational age: results from the Auckland Birthweight Collaborative study

  20843981   Associations of six single nucleotide polymorphisms in obesity-related genes with BMI and risk of obesity in Chinese children.

  20935630   Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

  21466928   Genetics and epigenetics of obesity.

  21602305   A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort.

  21912638   Studies of metabolic phenotypic correlates of 15 obesity associated gene variants.

  21935397   Genome-wide population-based association study of extremely overweight young adults--the GOYA study.

  21976109   Association of obesity-related genetic variants with endometrial cancer risk: a report from the Shanghai Endometrial Cancer Genetics Study.

  22043166   Gene-diet interactions in childhood obesity.

  22051089   Associations of obesity genes with obesity-related outcomes in multiethnic children.

  22430306   Evaluation of common genetic variants identified by GWAS for early onset and morbid obesity in population-based samples.

  23036011   Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases.

  23339409   Reduced genetic influence on childhood obesity in small for gestational age children.

  23471855   The genetics of childhood obesity and interaction with dietary macronutrients.

  23588626   Associations of obesity susceptibility loci with hypertension in Chinese children.

  23874820   Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression.

  24033266   A systematic approach to assessing the clinical significance of genetic variants.

  24269186   An obesity genetic risk score is associated with metabolic syndrome in Chinese children.

  24767253   Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders.

  25741868   Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

  26727462   Physical activity and genetic predisposition to obesity in a multiethnic longitudinal study.

  27480816   Longitudinal relationships between glycemic status and body mass index in a multiethnic study: evidence from observational and genetic epidemiology.

  27549128   An uncommon inheritance pattern in Niemann-Pick disease type C: identification of probable paternal germline mosaicism in a Mexican family.

  27900365   Genome sequencing in a case of Niemann-Pick type C.

  28123713   Association between the rs1805081 polymorphism of Niemann-Pick type C1 gene and cardiovascular disease in a sample of an Iranian population.

  28636007   Analysis of association of gene variants with obesity traits in New Zealand European children at 6 years of age.

  28693089   [Effect of genetic polymorphisms on change in body mass index and obesity status during childhood].

  30458724   Association of Uncoupling Protein 1 (UCP1) gene polymorphism with obesity: a case-control study.

  23757202   Free the data: one laboratory's approach to knowledge-based classification of genomic variants and preparation for integration of genomic data into EMR.

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