Table 3 |
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|
Linkage results with P-values ≤ 0.0017 (suggestive evidence) for at least one method of analysis from quantitative and qualitative analyses of the total Social Responsiveness Score (SRS). |
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|
Chromosome |
Location1 |
Score (alpha2; P-value) |
Phenotype, model |
|
|
|||
|
6p25.3 |
133,969 |
1.93 (0.40; 0.0014) |
Qualitative, recessive |
|
|
|||
|
6p22.1 |
26,261,314 |
2.36 (0.31; 0.00049) |
Qualitative, recessive |
|
|
|||
|
7q31.1-q32.3 |
113,934,453 |
2.07 (0.54; 0.001) |
Quantitative, parametric |
|
|
|||
|
129,451,548 |
2.91 (--; 0.00013) |
Quantitative, NPL |
|
|
|
|||
|
130,291,151 |
2.55 (0.37; 0.00031) |
Qualitative, recessive |
|
|
|
|||
|
9p24.33 |
593,192 |
2.66 (0.75; 0.00023) |
Quantitative, parametric |
|
|
|||
|
10p12.1 |
27,770,267 |
2.03 (0.74; 0.0011) |
Qualitative, dominant |
|
|
|||
|
10q22.1-q22.2 |
76,287,863 |
1.88 (0.65; 0.0016) |
Qualitative, dominant |
|
|
|||
|
11p15.1-p15.44 |
12,519,296 |
2.77 (0.44; 0.00018) |
Quantitative, parametric |
|
|
|||
|
13q12.3 |
30,070,594 |
2.23 (0.60; 0.00068) |
Qualitative, recessive |
|
|
|||
|
13q32.1 |
94,452,168 |
2.14 (0.85; 0.00085) |
Qualitative, recessive |
|
|
|||
|
15q13.3 |
31,177,959 |
3.64 (--; 0.000021) |
Qualitative, NPL |
|
|
|||
|
31,177,959 |
3.07 (0.70; 0.000085) |
Qualitative, recessive |
|
|
|
|||
|
19q13.43 |
59,338,102 |
2.14 (0.71; 0.00085) |
Quantitative, parametric |
|
|
|||
|
Bold font indicates significant evidence (P ≤ 0.000048). Note: All nonparametric linkage (NPL) scores have been converted to equivalent logarithm of the odds (LOD) scores. Chromosomal locations indicated in italics overlap our affected-only genome scan using clinical diagnosis [32]. 1 Location at the maximum of the peak. 2 Alpha, the estimated proportion of linked families for the MCLINK heterogeneity LOD score, is given for parametric analyses. 3 The peak at 9p24.3 is in the same location as a peak reported in a single family from our sample [35]. 4 The peak at 11p15.1-p15.4 replicates previous genome scan results of quantitative SRS scores [20]. |
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|
Coon et al. Molecular Autism 2010 1:8 doi:10.1186/2040-2392-1-8 |
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