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. 2021 Mar 5;12:639226. doi: 10.3389/fimmu.2021.639226

Table 4.

Haplotype study.

Microsatellite marker D1S212 D1S2751 D1S2640 D1S2619 D1S2623 Mutation D1S2701 D1S2711 D1S202 D1S238
Chromosome position 178082616 180011174 180727202 182276183 182873602 Mutation 184622684 185417782 186865356 188146265
Patient H1 111/111 238/238 185/185 183/183 278/278 Homozygous 129/129 151/151 81/81 268/268
N4 109/109 234/234 185/185 183/183 278/278 Homozygous 129/129 155/155 73/73 282/282
O3 109/115 234/240 185/187 185/185 278/278 Homozygous 129/129 151/151 83/83 284/284
P1 111/111 232/232 185/185 183/183 278/278 Homozygous 129/129 155/155 81/81 270/284
AK4 109/109 238/238 185/185 183/183 278/278 Homozygous 129/129 151/151 81/81 270/270
AM2 109/109 230/230 185/185 179/179 276/276 Homozygous 127/127 155/155 79/79 282/282
AN2 107/107 238/238 197/197 183/183 278/278 Homozygous 129/129 151/151 83/83 280/280
Q3 107/109 234/236 185/187 183/183 278/278 Homozygous 129/129 155/155 73/73 282/282

Marker encompassing NCF2 with chromosome 1 position based on hg19 are shown. The founder haplotype is shaded in gray.