|
HT
|
c.129C>T
|
IVS2 533 G>A
|
c.677C>T
|
c.1068C>T
|
IVS10 262C>G
|
1298A
|
1298C
|
|---|
|
1
|
C
|
G
|
C
|
C
|
C
|
0.3201
|
0.1043
|
|
2
|
C
|
G
|
T
|
C
|
C
|
0.2956
|
0
|
|
3
|
C
|
G
|
T
|
C
|
G
|
0.1113
|
0
|
|
4
|
C
|
G
|
C
|
C
|
G
|
0.1026
|
0.2287
|
|
5
|
C
|
A
|
T
|
C
|
C
|
0.0661
|
0
|
|
6
|
C
|
A
|
C
|
C
|
G
|
0.0432
|
0.3468
|
|
7
|
C
|
A
|
T
|
C
|
G
|
0.0384
|
0
|
|
8
|
T
|
A
|
C
|
C
|
C
|
0.0114
|
0.1279
|
|
9
|
C
|
G
|
C
|
T
|
C
|
0.0114
|
0.1128
|
|
10
|
T
|
G
|
C
|
T
|
C
|
0
|
0.0390
|
|
11
|
T
|
A
|
C
|
T
|
C
|
0
|
0.0160
|
|
12
|
T
|
G
|
C
|
T
|
C
|
0
|
0.0122
|
|
13
|
C
|
G
|
T
|
T
|
C
|
0
|
0.0122
|
- Haplotypes with an estimated frequency below 0.01 are not shown. Numbering refers to haplotypes of c.1298A alleles (1-13; the additional c.1298 haplotypes not observed in c.1298A (C) alleles were numbered consecutively regarding their frequency). Frequencies are shown as the ratio of total amount of each 1298A and 1298C-alleles.
