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Article

A haplotype map of the human genome.

Nature - 27 Oct 2005

Abstract excerpt

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...

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Share to Chromosomes, Human, Y
Share to DNA, Mitochondrial
Share to Gene Frequency

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genome, Human

Share to Haplotypes

Share to Linkage Disequilibrium

Share to Recombination, Genetic

Share to Selection, Genetic

Source

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Identifiers

PMID: 16255080
DOI: 10.1038/nature04226
PMCID: PMC1880871

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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