rs1619561

This variant is located in the PITPNM2 gene.

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GWAS Catalog Trait Associations (1)

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

Tourette syndrome, educational attainment

Chen D et al. “Unraveling shared susceptibility loci and Mendelian genetic associations linking educational attainment with multiple neuropsychiatric disorders.” Frontiers in Psychiatry 14:1303430 (2023)

Allele C

OR —

p 6.0e-15

N 308,030

Large GWAS

European

About PITPNM2

PITPNM2 belongs to a family of membrane-associated phosphatidylinositol transfer domain-containing proteins that share homology with the Drosophila retinal degeneration B (rdgB) protein (Ocaka et al., 2005 [PubMed 15627748]).[supplied by OMIM, Mar 2008]

View all PITPNM2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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