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Article

SNP discovery in associating genetic variation with human disease phenotypes.

Mutation research - 3 Jun 2005

Suh Yousin, Vijg Jan

Abstract excerpt

With the completion of the human genome project, attention is now rapidly shifting towards the study of individual genetic variation. The most abundant source of genetic variation in the human genome is represented by single nucleotide polymorphisms (SNPs), which can account for heritable inter-individual differences in complex phenotypes. Identification of SNPs that contribute to susceptibility to common...

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PMID: 15829236
DOI: 10.1016/j.mrfmmm.2005.01.005

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

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