rs35718474

This is a protein-altering variant in the PRTG gene.

GWAS Catalog Trait Associations (1)

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

level of protogenin in blood

Allele A
OR 0.27
p 2.0e-15
N 47,745
Large GWAS
European

About PRTG

This gene encodes a member of the immunoglobulin superfamily. The encoded transmembrane protein has been associated with the development of various tissues, especially neurogenesis. It has been suggested that this gene may be associated with attention deficit hyperactivity disorder (ADHD). [provided by RefSeq, Nov 2014]

View all PRTG variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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