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. 2018 Feb 14;13(2):e0192696. doi: 10.1371/journal.pone.0192696

Table 2. Regions with significant linkage MMLS.

Position
(cM)
Phenotype; DRB1 Stratum MMLS LOD α (%) p-value
Chromosome 1p36.12
49 Unstratified T1D 3.94 -90 17 NA
45 Unstratified Complications 1.23 -9.82 26
49 Unstratified No complications 1.42 -59.31 13
Chromosome 1q32.1
215 T1D: 3/{3,X} 0.00 -54 0 14.09;
2.0e-4
210 Complications: 3/{3,X} 3.02 2.79 89
215 No complications: 3/{3,X} 0.04 -32 4
Chromosome 8q21.3
94 T1D: 3/{3,X} 2.31 -35.81 16 3.04
(0.08)
100 Complications: 3/{3,X} 2.88 2.02 64
94 No complications: 3/{3,X} 0.09 -14 10
Chromosome 12p11.21
61 T1D:X/X 1.66 -11 26 7.23
(0.007)
54 Complications: X/X 0.02 -1.54 13
57 No complications: X/X 3.21 -0.09 52
Chromosome 22q11.21
12 T1D:3/4 3.24 -1.39 56 1.43
(0.23)
17 Complications:3/4 2.22 2.22 100
11 No complications:3/4 1.33 -4.00 43

Maximum MMLS, LOD, and estimated linked percentage of pedigrees (α) observed for the three phenotypes, T1D, Complications and No complications, only for the DRB1 allele strata corresponding to each linkage peak above 3.0. The last column contains the significance p-value of the pre-divided sample test.