Table 1.
SNP position in haplotype | SNP ida | Chromosome position | Database id | SNP genomic location | COMMON allele (minor allele) | Allele frequency |
---|---|---|---|---|---|---|
1 | AFP+8865 | 74300068 | rs2298839 | intron/exon | A(g) | 0.41 |
2 | AFM+1666 | 74338382 | rs1894292 | intron | A(g) | 0.24 |
3 | AFM+4530 | 74341246 | rs1894293 | intron | G(a) | 0.33 |
4 | AFM+15790 | 74352506 | rs1158101 | intron/exon | C(t) | 0.14 |
5 | IL8-251 | 74595248 | rs4073 | promoter | A(T) | 0.14 |
6 | IL8+396 | 74595893 | rs2227307 | intron | T(g) | 0.47 |
7 | IL8+37674 | 74633165 | rs13109146 | flanking | C(t) | 0.04 |
8 | IL8+39739 | 74635230 | rs39739 | flanking | G(a) | 0.04 |
9 | IL8+40050 | 74635538 | rs2224434 | flanking | C(a) | 0.14 |
a SNPs given in bold were selected for typing in the complete sample set of 651 case-control pairs.