rs73058052

This variant is located in the PRR12 gene.

GWAS Catalog Trait Associations (2)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

circulating fibrinogen levels

Allele T
OR
β 0.007
p 2.0e-8
N 120,246
Meta-analysisLarge GWAS
European

ClinVar annotation

Benign★★★
3 submitters1 publication

not provided; PRR12-related disorder

View on ClinVar →

About PRR12

This gene encodes a proline-rich protein that contains two A-T hook DNA binding domains. A chromosomal translocation and gene fusion between this gene and zinc finger, MIZ-type containing 1 (Gene ID: 57178) may underlie intellectual disability and neuropsychiatric problems in a human patient. Enriched expression of this gene in embryonic mouse brain suggests that this gene may play a role in nervous system development. [provided by RefSeq, Jul 2016]

View all PRR12 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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