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. 2021 Jun 15;12:689897. doi: 10.3389/fgene.2021.689897

Table 4.

The 15 single-nucleotide polymorphisms (SNPs) used as instrumental variables of obsessive compulsive disorder (OCD).

rsID Nearest gene Effect allele β se p-value Secondary phenotype*
rs1030757 GRID2 A 0.847639 0.0339 1.09E-06 /
rs116347760 MAGI3 A 1.87705 0.1335 2.39E-06 /
rs117310268 RP11-595B24.2 T 1.56627 0.0965 3.31E-06 /
rs12504244 NMU C 0.844593 0.0352 1.62E-06 Myeloid white cell count
rs12568997 RN7SL583P A 0.745798 0.058 4.23E-07 /
rs13141765 RP11-586D19.1 T 0.766209 0.0558 1.86E-06 /
rs4733767 CASC8 A 1.21349 0.039 7.10E-07 /
rs55687617 RP11-10F11.3 A 0.763227 0.0575 2.67E-06 /
rs56343802 AHCYP4 A 0.843834 0.0368 3.97E-06 /
rs639560 PLA2G4D T 0.659812 0.0879 2.23E-06 /
rs72781967 RP13-463N16.6 T 0.846538 0.0353 2.43E-06 /
rs72783425 MKL2 A 1.40453 0.0733 3.53E-06 /
rs77885126 RP11-325K19.1 T 0.547441 0.1312 4.38E-06 /
rs909701 LINC00207 C 0.856073 0.0337 4.05E-06 /
rs9952159 DLGAP1 T 1.19997 0.0396 4.21E-06 /
*

Secondary phenotypes were detected by PhenoScanner (www.phenoscanner.medschl.cam.ac.uk), with filtration of p < 5 × 10−8 and r2 > 0.8.

rsID, the ID of the single nucleotide polymorphism (SNP); β, the effect size of the SNP; se, the standard error of the effect size.