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Article

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.

Nature genetics - 1 Apr 2001

Glatt C E, DeYoung J A, Delgado S, Service S K, Giacomini K M, Edwards R H, Risch N, Freimer N B

Abstract excerpt

Most human sequence variation is in the form of single-nucleotide polymorphisms (SNPs). It has been proposed that coding-region SNPs (cSNPs) be used for direct association studies to determine the genetic basis of complex traits. The success of such studies depends on the frequency of disease-ass...

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PMID: 11279528
DOI: 10.1038/86948

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-11279528-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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