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SNP information rs7023329

RS7023329

Normal allele: GG

Polymorphism rs7023329 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:

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

  19578365   Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.

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

  20546537   Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis.

  20574843   Associations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutations.

  20585100   Genome-wide association studies of cancer.

  20647408   Melanocytic nevi, nevus genes, and melanoma risk in a large case-control study in the United Kingdom.

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

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

  21962134   Polymorphisms in nevus-associated genes MTAP, PLA2G6, and IRF4 and the risk of invasive cutaneous melanoma.

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

  22034633   Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1.

  23361049   Common genetic variants in the 9p21 region and their associations with multiple tumours.

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

  26732429   Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.

  27079684   Genome-wide association studies and epigenome-wide association studies go together in cancer control.

  27229762   Genetic scores based on risk-associated single nucleotide polymorphisms (SNPs) can reveal inherited risk of renal cell carcinoma.

  27479139   Characterization of the Methylthioadenosine Phosphorylase Polymorphism rs7023954 - Incidence and Effects on Enzymatic Function in Malignant Melanoma.

  27960044   Genetic variants at 9p21.3 are associated with risk of esophageal squamous cell carcinoma in a Chinese population.

  33342058   Influence of germline genetic variants on dermoscopic features of melanoma.

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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