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Article

CLIA-tested genetic variants on commercial SNP arrays: potential for incidental findings in genome-wide association studies.

Genetics in medicine : official journal of the American College of Medical Genetics - 1 Jun 2010

Johnson Andrew D, Bhimavarapu Anupama, Benjamin Emelia J, Fox Caroline, Levy Daniel, Jarvik Gail P, O'Donnell Christopher J

Abstract excerpt

PURPOSE: Increases in throughput and affordability of genotyping products have led to large sample sizes in genetic studies, increasing the likelihood that incidental genetic findings may occur. We set out to survey potential notifiable variants on arrays used in genome-wide association studies and in direct-to-consumer genetic services. METHODS: We used multiple bioinformatics strategies to identify, and map...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 20556870
DOI: 10.1097/GIM.0b013e3181e1e2a9
PMCID: PMC3056880

Genes

APOE
BTD
GALT
HFE
MEFV
SPINK1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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