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SNP information rs1393350

RS1393350

Normal allele: GG

Polymorphism rs1393350 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:

  18483556   A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.

  19340012   Genome-wide association study of tanning phenotype in a population of European ancestry.

  19384953   Genetic variants in pigmentation genes, pigmentary phenotypes, and risk of skin cancer in Caucasians.

  19578364   Genome-wide association study identifies three loci associated with melanoma risk.

  19863770   Moderate- to low-risk variant alleles of cutaneous malignancies and nevi: lessons from genome-wide association studies.

  20410501   Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.

  20463881   Digital quantification of human eye color highlights genetic association of three new loci.

  20505153   A compendium of genome-wide associations for cancer: critical synopsis and reappraisal.

  20585100   Genome-wide association studies of cancer.

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

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

  21219822   [Recent progress in genetic variants associated with cancer and their implications in diagnostics development].

  21221757   ASIP genetic variants and the number of non-melanoma skin cancers.

  21674838   Genetic examination of the putative skull of Jan Kochanowski reveals its female sex.

  21926416   Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.

  21983787   Genome-wide association study identifies three new melanoma susceptibility loci.

  22629401   Evaluation of genetic markers as instruments for Mendelian randomization studies on vitamin D.

  22988944   Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.

  23927501   Why it is hard to find genes associated with social science traits: theoretical and empirical considerations.

  23948321   Genetic analyses of the human eye colours using a novel objective method for eye colour classification.

  24274136   Biobanking across the phenome - at the center of chronic disease research.

  24631691   The effect of gender on eye colour variation in European populations and an evaluation of the IrisPlex prediction model.

  24880832   Collaborative EDNAP exercise on the IrisPlex system for DNA-based prediction of human eye colour.

  24924479   Skin pigmentation, sun exposure and vitamin D levels in children of the Avon Longitudinal Study of Parents and Children.

  24926819   Increased risk of developing cutaneous malignant melanoma is associated with variation in pigmentation genes and VDR, and may involve epistatic effects.

  25077817   Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions.

  25724930   IRF4, MC1R and TYR genes are risk factors for actinic keratosis independent of skin color.

  26547235   Crowdsourced direct-to-consumer genomic analysis of a family quartet.

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

  26870082   Genetic Susceptibility to Vitiligo: GWAS Approaches for Identifying Vitiligo Susceptibility Genes and Loci.

  27221533   Further evidence for population specific differences in the effect of DNA markers and gender on eye colour prediction in forensics.

  27468418   Importance of nonsynonymous OCA2 variants in human eye color prediction.

  32604780   Evaluation of the VISAGE Basic Tool for Appearance and Ancestry Prediction Using PowerSeq Chemistry on the MiSeq FGx System.

  34071952   Prediction of Eye Colour in Scandinavians Using the EyeColour 11 (EC11) SNP Set.

  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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