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Table 3 Results for BAP and secondary phenotypes for any locus with PPL >20% for at least one phenotype (US pedigrees only)

From: A molecular genetic study of autism and related phenotypes in extended pedigrees

Locus

cMa

Phenotype

  

BAP b

ANX

PRS

RRB

SOC

2q37.2-q37.3

248–264

0.59

0.37

0.08

0.00

0.14

6p25.3-p25.2

0–8

0.04

0.00

0.26

0.03

0.04

6p25.2-24.3

12–20

0.05

0.00

0.03

0.62

0.07

8q24.13

126–134

0.04

0.03

0.03

0.00

0.37

9p21.3

44–48

0.13

0.23

0.01

0.00

0.00

9q21.31-q22.31

80–98

0.11

0.06

0.41

0.00

0.54

11q23.2-q23.3

120–126

0.26

0.00

0.01

0.00

0.00

12q21.1-q21.33

90–102

0.24

0.03

0.10

0.05

0.27

13q11-q12.3

0–26

0.14

0.51

0.32

0.00

0.01

14q31.1-q32.13

78–96

0.27

0.00

0.10

0.00

0.00

15q13.2-q13.3

20–22

0.22

0.00

0.02

0.00

0.00

15q26.3

122–128

0.01

0.33

0.01

0.00

0.00

19p13.3

10–18

0.02

0.00

0.07

0.69

0.01

19p12-q12

48–54

0.02

0.00

0.03

0.00

0.32

22q13.31

58–60

0.00

0.00

0.03

0.00

0.21

  1. aThe cM region corresponds to the phenotype with the highest PPL, extending out to cover PPL >10% around that peak for any phenotype. PPLs for additional phenotypes represent the maximum within this region for the given phenotype. bNote that these represent PPLs based on the University of North Carolina (UNC) pedigrees only, and they are therefore not identical to results shown in Figure 2.