Multiple single nucleotide polymorphisms on human chromosome 19q13.2-3 associate with risk of Basal cell carcinoma

Cancer Epidemiol Biomarkers Prev. 2002 Nov;11(11):1449-53.

Abstract

In this paper, we present evidence that alleles of several polymorphisms in the chromosomal region 19q13.2-3, encompassing the genes RAI and XPD, are associated with occurrence of basal cell carcinoma in Caucasian Americans. The association of one of these, RAI-intron1, is sufficiently strong to make mass significance unlikely (P = 0.004, chi(2)). We interpret our combined data to indicate that a specific haplotype partly defined by the alleles of three single nucleotide polymorphisms, RAI intron1(G), RAI exon6(T), and XPD exon 6(C), is associated with a protective gene variant in a region spanning from XPD to ERCC1.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Biomarkers, Tumor / genetics
  • Carcinoma, Basal Cell / epidemiology*
  • Carcinoma, Basal Cell / genetics*
  • Chromosomes, Human, Pair 19 / genetics*
  • Exons / genetics
  • Family Health
  • Female
  • Gene Frequency / genetics
  • Genetic Predisposition to Disease / genetics
  • Genotype
  • Humans
  • Introns / genetics
  • Linkage Disequilibrium / genetics
  • Male
  • Middle Aged
  • Molecular Sequence Data
  • Polymorphism, Single Nucleotide / genetics*
  • Risk Factors
  • Sequence Analysis, DNA
  • Skin Neoplasms / epidemiology*
  • Skin Neoplasms / genetics
  • White People

Substances

  • Biomarkers, Tumor

Associated data

  • GENBANK/AC005781
  • GENBANK/AC008622
  • GENBANK/AC010519
  • GENBANK/L27710
  • GENBANK/L47234
  • GENBANK/M63796
  • GENBANK/M89651