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How valid is single nucleotide polymorphism (SNP) diagnosis for the individual risk assessment of breast cancer?

Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology - 1 Mar 2006

Tempfer Clemens B, Hefler Lukas A, Schneeberger Christian, Huber Johannes C

Abstract excerpt

The number of reports investigating disease susceptibility based on the carriage of low-penetrance, high-frequency single nucleotide polymorphisms (SNPs) has increased in recent years. Evidence is accumulating defining specific individual variations in breast cancer susceptibility. Genetic variations of estradiol and xenobiotics metabolisms as well as genes involved in cell-cycle control have been described as...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16835078
DOI: 10.1080/09513590600629175

Genes

GSTM1
TGFBR1
VDR
XRCC1
XRCC2

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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