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. 1998 Sep 1;95(18):10746–10750. doi: 10.1073/pnas.95.18.10746

Table 2.

Evidence for linkage (P < 0.05) from the RA genome scan performed with 309 markers outside of the HLA region

D number AFM* Position Region S NS P pM
D1S228 196xb4 32.4 1.1/1p36-pter 89.5 56.8 0.0035 0.0065
D1S238 205xg1 206.7 1.2/1q31-32 94.2 68.5 0.022 0.099
D2S380 321xd9 88.0 2.1/2p13-pter 102.1 78.7 0.041 0.010
D2S377 319zf9 228.2 2.2/2q33-37 84.9 61.0 0.024 0.013
D2S2354 a046we1 235.0 2.2 91.1 58.9 0.0043 0.0054
D3S1267 116xh2 141.1 3.1/3q13 96.1 63.4 0.032 0.039
D3S1262 059xa9 207.2 3.2/3q27 97.0 75.0 0.046 0.11
D5S422 211yc7 163.9 5.1/5q32-33 99.5 75.2 0.033 0.045
D6S292 203za9 138.2 6.1/6q21-23 89.0 66.7 0.036 0.034
D8S1825 a055zg1 14.9 8.1/8p23-pter 89.0 67.1 0.040 0.10
D12S99 217xa7 13.9 12.1/12p13-pter 66.5 41.4 0.0077 0.083
D12S95 207ve1 97.7 12.2/12p13-q24 67.4 41.6 0.0067 0.043
D13S170 240wh2 65.4 13.1/13q31 92.9 70.4 0.039 0.015
D13S1315 a058xd5 105.2 13.2/13q32-qter 110.4 65.4 0.00035 0.0037
D14S285 319vf5 50.0 14.1/14q13-23 57.5 41.1 0.049 0.33
D16S420 238xb2 43.2 16.1/16p12 70.2 51.8 0.047 0.039
D16S401 025tg9 45.5 16.1 56.9 34.0 0.0080 0.028
D16S516 350vd1 98.3 16.2/16q24 75.7 55.4 0.038 0.11
D16S511 312xd1 108.4 16.2 108.6 85.6 0.049 0.11
D18S57 147yg7 63.2 18.1/18q12 101.2 73.5 0.018 0.033
D18S474 295xh1 71.3 18.1 84.5 63.0 0.038 0.012
D18S68 248yb9 94.4 18.2/18q22-23 97.1 72.9 0.032 0.020
D18S61 193yf8 102.8 18.2 108.6 69.3 0.0016 0.0098
D18S469 116yg11 109.0 18.2 79.7 50.6 0.0055 0.020
D20S864 a343xc9 0.0 20.1/20pter 63.7 44.2 0.030 0.11
D21S270 031xc5 41.3 21.1/21q22-qter 97.0 73.7 0.038 0.11
D21S268 260ze9 44.3 21.1 96.4 71.0 0.025 0.13
D22S264 0–9 22.1/22q11 74.6 51.4 0.019 0.0098
DXS1068 238yo11 56.2 X.1/Xp11-21 34.8 21.9 0.044 0.27
DXS998 224zg11 183.8 X.2/Xq27 35.3 17.7 0.0078 0.019

Position on the chromosome is provided in cM from the telomere of the short arm, based on the Généthon linkage map (20). Candidate regions are numbered consecutively for each chromosome. Clusters of markers adjacent in the scan are assigned to a single region. The number of alleles IBD in affected sib pairs reported for each marker and the associated P value are calculated by the program sibpalna (S for shared, NS for not shared). The P value calculated by the multipoint analysis program genehunter (pM) is provided. The raw data for the genome scan are available on Généthon’s web site. 

*

Ref. 20