Table 1 R2100 Multipoint Linkage Analysis Result
From: Novel Usher syndrome pathogenic variants identified in cases with hearing and vision loss
Start | End | |||||
|---|---|---|---|---|---|---|
Chromosome | LOD | dbSNP | Position | dbSNP | Position | Size (Mb) |
1 | 0.58 | rs3933251 | 64,095,165 | rs591540 | 71,866,132 | 7.8 |
3 | 1.68 | rs1400207 | 2,825,953 | rs13084851 | 4,115,819 | 1.3 |
4 | 1.68 | rs7671597 | 41,665,756 | rs2035906 | 45,815,310 | 4.1 |
5 | 1.68 | rs12110158 | 78,378,722 | rs257239 | 97,997,738 | 19.6 |
6 | 1.67 | rs1322633 | 125,082,133 | rs1490388 | 126,514,509 | 1.4 |
11 | 1.64 | rs1320211 | 15,301,410 | rs10833818 | 22,795,026 | 7.5 |
15 | 1.68 | rs937302 | 33,627,848 | rs11070349 | 41,792,819 | 8.2 |
20 | 1.41 | rs237417 | 5,770,142 | rs4140471 | 7,226,740 | 1.5 |