Table 3.
SNP no. | Position in NT_02257.18* | IBD cases | Controls | ||||
---|---|---|---|---|---|---|---|
N alleles included | N variant alleles | Allele frequency in % | N alleles included | N variant alleles | Allele frequency in % | ||
1 | 12332979G>T | 566 | 0 | 0 | 364 | 1 | 0.27 |
2 | 12333068insC | 566 | 1 | 0.18 | 364 | 0 | 0 |
3 | 12333070C>T | 566 | 0 | 0 | 364 | 2 | 0.55 |
4 | 12333125C>G | 566 | 60 | 10.60 | 364 | 50 | 13.74 |
5 | 12333199T>G | 566 | 1 | 0.18 | 364 | 0 | 0 |
6 | 12333213G>A | 566 | 0 | 0 | 364 | 3 | 0.82 |
7 | 12361272C>T | 562 | 1 | 0.18 | 358 | 0 | 0 |
8 | 12361422A>G | 562 | 0 | 0 | 358 | 1 | 0.28 |
9 | 12363017A>G | 554 | 1 | 0.18 | 334 | 0 | 0 |
10 | 12374014G>T | 554 | 1 | 0.18 | 348 | 0 | 0 |
11 | 12374024A>T | 564 | 1 | 0.18 | 348 | 0 | 0 |
12 | 12374091C>A | 554 | 1 | 0.18 | 348 | 0 | 0 |
13 | 12374110C>T | 554 | 1 | 0.18 | 348 | 0 | 0 |
14 | 12374272A>T | 554 | 1 | 0.18 | 348 | 1 | 0.29 |
15 | 12374352C>T | 554 | 0 | 0 | 348 | 1 | 0.29 |
16 | 12387616G>A | 562 | 1 | 0.18 | 360 | 0 | 0 |
17 | 12398613C>T | 546 | 0 | 0 | 370 | 1 | 0.27 |
28 | 12415473G>A | 546 | 0 | 0 | 350 | 1 | 0.29 |
19 | 12415557C>T | 546 | 66 | 12.09 | 350 | 46 | 13.14 |
20 | 12415581G>A | 546 | 0 | 0 | 350 | 1 | 0.29 |
21 | 12415647G>A | 546 | 2 | 0.37 | 350 | 0 | 0 |
22 | 12415669C>T | 546 | 0 | 0 | 350 | 1 | 0.29 |
no.: number; N: absolute number; *DNA reference sequence signature in NCBI.