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Article

An in-house multilocus SNP genotyping assay for evaluation of complex genetic diseases.

Scandinavian journal of clinical and laboratory investigation - 1 Nov 2016

Shah Swarup A V, Kondkar Altaf A, Ashavaid Tester F

Abstract excerpt

BACKGROUND: With an increase in the discovery of newer genetic loci/polymorphisms in complex multifactorial diseases, there is also an increased need for methods that can simultaneously genotype multiple loci in a cost-effective manner. Using coronary artery disease (CAD) as a model, the study aimed to develop an in-house multilocus assay for simultaneous detection of 17 genetic variants in 11 genes implicated in...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 27562454
DOI: 10.1080/00365513.2016.1218535

Genes

CAD
CETP
LPL
AGT
CBS
FGB
ITGB3
LDLR
LIPC
MTR
NOS3

Variants

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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