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SNP information rs1805009

RS1805009

Normal allele: GG

Polymorphism rs1805009 is related to topics like this:

Melanoma genes

The incidence of malignant melanoma (MM) is rising sharply, making it one of the most aggressive...


Research and publications:

  7581459   Variants of the melanocyte-stimulating hormone receptor gene are associated with red hair and fair skin in humans.

  11179997   Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma.

  17616515   Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles.

  17999355   A genomewide association study of skin pigmentation in a South Asian population.

  18366057   MC1R variants, melanoma and red hair color phenotype: a meta-analysis.

  19710684   Multiple pigmentation gene polymorphisms account for a substantial proportion of risk of cutaneous malignant melanoma.

  20585627   Web-based, participant-driven studies yield novel genetic associations for common traits.

  20670983   The Multiple Sclerosis Severity Score: associations with MC1R single nucleotide polymorphisms and host response to ultraviolet radiation.

  21197618   Model-based prediction of human hair color using DNA variants.

  24809478   Implications of the admixture process in skin color molecular assessment.

  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.

  25945350   Variants of SCARB1 and VDR Involved in Complex Genetic Interactions May Be Implicated in the Genetic Susceptibility to Clear Cell Renal Cell Carcinoma.

  26848990   Biochip-Based Genotyping Assay for Detection of Polymorphisms in Pigmentation Genes Associated with Cutaneous Melanoma.

  30657907   A study in scarlet: MC1R as the main predictor of red hair and exemplar of the flip-flop effect.

  35176104   Unveiling forensically relevant biogeographic, phenotype and Y-chromosome SNP variation in Pakistani ethnic groups using a customized hybridisation enrichment forensic intelligence panel.

Genetic testing for cancer

Medical tests are employed to detect specific changes or mutations in an individual's genes and...

Colorectal cancer genes

One of the prevalent cancer syndromes that can be inherited is colon cancer. Chromosome 2 contains...

Gastrointestinal tract cancer

The occurrence of gastrointestinal (GI) tract cancers caused by genetic mutations is widespread...

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