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.