rs140681152

This is a downstream gene variant variant in the PRPF31 gene.

GWAS Catalog Trait Associations (1)

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

About PRPF31

This gene encodes a component of the spliceosome complex and is one of several retinitis pigmentosa-causing genes. When the gene product is added to the spliceosome complex, activation occurs.[provided by RefSeq, Jan 2009]

View all PRPF31 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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