Ontology highlight
ABSTRACT:
SUBMITTER: International HapMap Consortium
PROVIDER: S-EPMC1880871 | biostudies-literature | 2005 Oct
REPOSITORIES: biostudies-literature
Nature 20051001 7063
Inherited genetic variation has a critical but as yet largely uncharacterized role in human disease. Here we report a public database of common variation in the human genome: more than one million single nucleotide polymorphisms (SNPs) for which accurate and complete genotypes have been obtained in 269 DNA samples from four populations, including ten 500-kilobase regions in which essentially all information about common DNA variation has been extracted. These data document the generality of reco ...[more]