HaploX PregCipher Genetic Test detects 558 genes associated with 550 genetic congenital diseases to identify individuals at risk of having a child with genetic conditions such as hereditary hearing loss. It provides insights into their carrier status for pathogenic variations.
1. Individuals with fertility intention/in reproductive age.
2. Individuals with a family history of genetic diseases.
3. Individuals with a history of adverse reproductive outcomes.
4. Couples who are seeking to conceive through assisted reproductive technology.
5. Couples with close blood relations.