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Article

A high density SNP genotyping approach within the 19q13 chromosome region identifies an association of a CNOT3 polymorphism with ankylosing spondylitis.

Annals of the rheumatic diseases - 1 May 2012

Díaz-Peña Roberto, Aransay Ana M, Suárez-Álvarez Beatriz, Bruges-Armas Jacome, Rodríguez-Ezpeleta Naiara, Regueiro María, Pimentel-Santos Fernando M, Mulero Juan, Sánchez Alejandra, Collantes Eduardo, Queiro Rubén, Ballina Javier, Alves Helena, López-Larrea Carlos

Abstract excerpt

OBJECTIVE: To identify genomic variants in the 19q13 chromosome region associated with ankylosing spondylitis (AS) in human leucocyte antigen (HLA)-B27-positive populations. METHODS: High-throughput genotyping of 1536 haplotype-tag single nucleotide polymorphisms (SNPs) was performed in 249 patie...

Read the complete abstract on PubMed

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Share to Chromosomes, Human, Pair 19
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to High-Throughput Screening Assays

Share to HLA-B27 Antigen

Share to Polymorphism, Single Nucleotide

Share to Receptors, Immunologic

Share to Spondylitis, Ankylosing

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Source

Identifiers

PMID: 22294640
DOI: 10.1136/annrheumdis-2011-200661

Genes

CNOT3
LAIR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22294640-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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