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Article

SNP alleles in human disease and evolution.

Journal of human genetics - 1 Jan 2002

Shastry Barkur S

Abstract excerpt

In two randomly selected human genomes, 99.9% of the DNA sequence is identical. The remaining 0.1% of DNA contains sequence variations. The most common type of such variation is called a single-nucleotide polymorphism, or SNP. SNPs are highly abundant, stable, and distributed throughout the genome. These variations are associated with diversity in the population, individuality, susceptibility to diseases, and...

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PMID: 12436191
DOI: 10.1007/s100380200086

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