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Article

Classifying single nucleotide polymorphisms in humans.

Molecular genetics and genomics : MGG - 1 Sept 2021

Azizzadeh-Roodpish Shima, Garzon Max H, Mainali Sambriddhi

Abstract excerpt

Single nucleotide polymorphisms (SNPs) are the most common form of genetic variation amongst the human population and are key to personalized medicine. New tests are presented to distinguish pathogenic/malign (i.e., likely to contribute to or cause a disease) from nonpathogenic/benign SNPs, regardless of whether they occur in coding (exon) or noncoding (intron) regions in the human genome. The tests are based on...

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Identifiers

PMID: 34259913
DOI: 10.1007/s00438-021-01805-x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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