Table 2.
Genotyping for a sex associated marker, amelogenin (AMEL), and 10 short tandem repeats to confirm paternity and maternity of an individual with Schnyder corneal dystrophy.
| Allelic marker | Father (I/1)∗ | Child (II/2)∗ | Mother (I/2)∗ | Random match probability | |||
|---|---|---|---|---|---|---|---|
| AMEL | Y | X | X | X | X | X | N/A |
| CSF1PO | 11 | 10 | 10 | 10 | 10 | 12 | 0.112 |
| D13S317 | 11 | 9 | 9 | 12 | 12 | 11 | 0.085 |
| D16S539 | 11 | 9 | 9 | 11 | 11 | 12 | 0.089 |
| D21S11 | 32.2 | 30 | 30 | 28 | 28 | 30 | 0.039 |
| D5S818 | 11 | 11 | 11 | 12 | 12 | 12 | 0.158 |
| D7S820 | 12 | 8 | 8 | 9 | 9 | 12 | 0.065 |
| TH01 | 6 | 6 | 6 | 6 | 6 | 9 | 0.081 |
| TPOX | 9 | 10 | 10 | 11 | 11 | 11 | 0.195 |
| VWA | 14 | 17 | 17 | 18 | 18 | 14 | 0.062 |
Note: there is greater than 99.999% percent probability that both parents are the biological parents.
∗IDs in parenthesis refer to pedigree in Figure 1.