Table 2.
SNP | CHR | BP | Description and Nominated Gene(s) | PF p value | PF beta | SM p value | SM beta | Genotyped or Imputed |
---|---|---|---|---|---|---|---|---|
rs2046315 | 8 | 90280216 | Top hit for SM, no gene | 6.50E-7 | 1.87 | 7.85E-8 | 5.19 | Genotyped |
rs17145638 | X | 39770574 | Top hit for PF, BCOR | 1.79E-7 | -2.33 | .001 | -3.85 | Genotyped |
rs10486722 | 7 | 41778433 | Suggestive hit for PF, INHBA | 6.50E-6 | 1.22 | .009 | 1.81 | Genotyped |
rs3788848 | X | 129027493 | Suggestive hit for SM, BCORL1 | .015 | 0.82 | 1.01E-5 | 3.81 | Genotyped |
rs1079204 | 2 | 218838758 | Suggestive hit for SM, CXCR1 and CXCR2 | .006 | 1.92 | 1.90E-6 | 8.45 | Imputed |
Associations shown in this Table are all of the same direction for PF and SM surfaces. Top hit: SNP with the smallest p value in a scan. Suggestive hit: SNP with p value less than 5E-5 in a scan.