SNP position in haplotype A or B
|
SNP ida
|
Chromosome position
|
Database id
|
SNP genomic location
|
COMMON allele (minor allele)
|
Allele frequency
|
---|
1A
|
IL3_2069783
|
131471923
|
rs2069783
|
5'UTR
|
T(c)
|
0.18
|
2A
|
IL3_31480
|
131472548
|
rs31480
|
5'UTR
|
G(a)
|
0.05
|
3A
|
IL3_40401
|
131472694
|
rs40401
|
exon
|
C(t)
|
0.45
|
4A
|
IL3_31481
|
131473418
|
rs31481
|
intron
|
G(a)
|
0.14
|
5A
|
CSF2_27348
|
131483355
|
rs27348
|
3'UTR
|
T(a)
|
0.39
|
6A
|
CSF2_2069614
|
131483817
|
rs2069614
|
3'UTR
|
T(c)
|
0.45
|
7A
|
CSF2_27438
|
131489471
|
rs27438
|
3'UTR
|
A(g)
|
0.23
|
8A
|
CSF2_2069632
|
131489516
|
rs2069632
|
3'UTR
|
C(t)
|
0.27
|
1B
|
IL13_46457
|
132072180
|
rs20541
|
exon
|
C(t)
|
0.14
|
2B
|
IL13_46578
|
132072059
|
rs1295686
|
splice site
|
A(g)
|
0.27
|
3B
|
IL13_49612
|
132069025
|
rs1800925
|
5'UTR
|
G(a)
|
0.40
|
4B
|
IL4-589
|
132085370
|
rs2243250
|
5'UTR
|
T(c)
|
0.27
|
5B
|
IL4+33
|
132085926
|
rs2070874
|
exon
|
C(t)
|
0.49
|
6B
|
IL4_2243251
|
132086003
|
rs2243251
|
5'UTR
|
T(c)
|
0.19
|
7B
|
IL4_2227284
|
132088941
|
rs2227284
|
intron
|
A(c)
|
0.05
|
8B
|
IL4_2243270
|
132090325
|
rs2243270
|
intron
|
C(t)
|
0.27
|
- SNPs given in bold were selected for typing in the complete sample set of 651 case-control pairs
-
aSNPs given in bold were selected for typing in the complete sample set of 651 case-control pairs.