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. 2005 Dec 30;6(Suppl 1):S128. doi: 10.1186/1471-2156-6-S1-S128

Table 2.

The most significant SNPs identified by FBAT. Empirical variance was used to estimate the p-value.

Chrom SNP position (cM) freq p value of (HWE) No. of fam Sa E(S)b Var(S)c Zd p-valuee
1 tsc0616094 68.9 0.868 1.0 41 221 202.4 26.6 3.6 0.000305
1 tsc0668988 99.4887 0.37 0.39 55 121 146.7 55.2 -3.5 0.000552
1 tsc1177811 105.535 0.318 0.13 53 83 105.4 43.5 -3.4 0.000682
3 f tsc0515272 164.236 0.876 0.02 45 248 223.4 29.6 4.5 0.000006
4 tsc0571248 172.977 0.223 0.26 54 79 102.2 49.6 -3.3 0.000988
5 tsc0158479 95.668 0.063 0.50 35 27 43.9 20.6 -3.7 0.000198
6 tsc1175206 127.576 0.675 0.59 59 279 252.9 52.6 3.6 0.000327
6 tsc0608218 146.124 0.184 0.61 48 63 81.7 31.4 -3.3 0.000839
9 tsc0048697 13.7398 0.342 0.87 54 113 135.5 46.2 -3.3 0.000935
11 tsc0569292 6.78451 0.788 0.02 40 191 173 27.3 3.5 0.00055
11 tsc0919042 81.1855 0.15 0.75 49 65 88.5 44.7 -3.5 0.000444
13 tsc0271621 60.1748 0.173 0.59 46 55 81.3 59.5 -3.4 0.000659
13 tsc0056748 73.9934 0.191 1.0 42 28 49.4 28.1 -4.0 0.000053
14 tsc0902508 81.2799 0.14 0.39 40 46 64.9 30.7 -3.4 0.000639
15 tsc0058074 49.9916 0.556 0.89 75 300 331.9 86.3 -3.4 0.000599
16 tsc1750530 59.8297 0.107 0.02 46 44 69.7 45.8 -3.8 0.000147
19 tsc0061923 66.8126 0.885 1.0 26 145 161.1 21.6 -3.5 0.000512
19 tsc0598556 102.054 0.664 0.26 63 335 304.3 73.9 3.6 0.000347
20 tsc0060446 35.4473 0.2 1.0 63 90 118.4 43.2 -4.3 0.000015
7 tsc0331830g 33.9373 0.113 1.0 39 59 74.2 31.5 -2.7 0.0067
7 tsc0593964g 42.6174 0.629 0.53 70 332 305.8 79.2 2.9 0.00328
7 tsc0042959g 44.4931 0.136 0.47 49 57 77.9 50.7 -2.9 0.003313
7 tsc0051325g 44.5631 0.749 0.58 61 284 309.8 79.5 -2.8 0.003754
7 tsc0797235g 122.213 0.897 0.71 37 231 214.6 37.6 2.7 0.007624

a Observed FBAT statistic based on a linear combination of offspring genotypes and traits.

b Estimated mean of S.

c Estimated variance of S.

d Z score defined by (S - E(S))/graphic file with name 1471-2156-6-S1-S128-i1.gif.

e No multiple comparison was corrected.

f Bold text indicates that the SNP achieves genome-wide significance.

g These SNPs listed because of linkage evidence observed on chromosome 7.