TABLE 4

Markers with evidence for linkage (P ≤ 0.001) in the 10-cM genome scan

Positive markersInterval*Position (cM)TraitsMLB LOD (P)MLS LOD (P)PCORR§PUNCORR§1-LOD unit (CI) (cM)
D2S3252q35215.26PCT992.77 (0.0002)3.26 (0.0001)0.160.0820.83 (222.1–242.9)
D6S2876q22.31124.49PCT973.61 (0.00002)4.29 (0.000009)0.010.0117.03 (128.2–145.2)
D6S2876q22.31124.49PCT953.08 (0.00008)3.62 (0.00005)0.080.0617.03 (128.2–145.2)
D6S2876q22.31124.49PCT992.07 (0.001)2.33 (0.001)0.450.3729.00 (125.3–154.3)
D15S100715q1426.78AAR2.11 (0.0009)NA0.730.3417.83 (23.9–41.8)
D16S51616q23.1112.09AAR2.08 (0.001)NA0.740.3531.43 (87.78–119.21)
D19S22619p13.1243.34AAR2.08 (0.001)NA0.740.3523.58 (26.2–49.8)
  • *

    * Chromosomes locations were determined from the map available in the Human Genome Browser.

  • Haldane’s distances were used to determine the locations of linkage peaks.

  • P: single-test P value;

  • §

    § PCORR: empirical genome-wide P value when considering all the traits; PUNCORR: empirical genome-wide P value when considering one trait only. NA, not available. A Genethon map was used.