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. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Hum Genet. 2013 Oct 1;133(2):173–186. doi: 10.1007/s00439-013-1370-8

Table 2.

Number of SNPs included in each prediction analysis

SNPs overlapping with NTR/NESDA SNPs overlapping between all three samples

P-value threshold RADIANT ATM (all) ATM (exMDD) RADIANT ATM (all) ATM (exMDD)
0.01 4,657 2,564 2,585 2,615 2,345 2,354
0.05 21,747 12,673 12,596 12,069 11,629 11,575
0.1 43,046 25,444 25,253 23,819 23,385 23,218
0.2 85,330 50,453 50,185 47,374 46,324 46,112
0.3 126,854 75,441 75,397 70,273 69,334 69,219
0.4 168,637 100,402 100,348 93,272 92,303 92,223
0.5 210,168 125,291 125,199 115,982 115,221 115,103
0.6 251,509 150,347 150,034 138,720 138,303 137,932
0.7 292,601 175,040 174,868 161,419 161,029 160,820
0.8 333,739 199,809 199,747 184,041 183,776 183,676
0.9 374,973 225,035 224,827 207,025 206,942 206,739
1.0 416,030 249,917 249,917 229,778 229,778 229,778

The number of SNPs used in the prediction analyses, for each P-value threshold. On the left the numbers for the set of SNPs in each sample that overlapped with the NTR-NESDA target sample (as used in the analyses presented in Figure 1), on the right the numbers for the set of SNPs that overlapped between all three samples (as used in the analyses presented in Figure 4).