rs2032562

rs2032562 is a single nucleotide polymorphism (SNP) in the human genome, identified by the rsID rs2032562 in the dbSNP database. As with other SNPs, its precise genomic location and functional context depend on the reference genome assembly (for example GRCh37/hg19 or GRCh38/hg38). In different annotations it may lie within an intron, exon, or intergenic region, and it may be located near one or more genes.

The two principal alleles of rs2032562 are recorded in population-scale datasets, with allele frequencies that differ among populations. Databases such as gnomAD provide population-specific frequencies for this SNP, reflecting the diversity of human genomes.

Associations between rs2032562 and traits or diseases have been investigated in genetic studies. As with many SNPs, reported associations may vary by study and population, and robust replication and meta-analysis are typically required to establish a reliable link.

In practice, rs2032562 is used as a genetic marker in research contexts and can be queried in resources including dbSNP, Ensembl, the GWAS Catalog, and population allele-frequency databases. The rsID provides a universal reference across genomic databases, but exact coordinates and annotations should be confirmed against the latest genome builds and annotation releases.