Male
| Variant Name | Allele Count | Allele Frequency | Associated Disease | Associated Gene |
|---|---|---|---|---|
| NC_000007.14:g.39545812T>C | ||||
| NC_000007.14:g.39531242G>A | ||||
| NM_207362.2:c.2416+3448C>T | ||||
| NM_207362.2:c.541-1069T>C | ||||
| NM_207362.2:c.70+169C>A | ||||
| NM_207362.2:c.-10-2145G>A | ||||
| NM_207362.2:c.-10-3458C>T |