What exactly is carrier screening?
Carrier screening is a type of genetic test that can tell you whether you carry a gene for certain genetic disorders. When it is done before or during pregnancy, it allows you to find out the chances of having a child with a genetic disorder like Cystic Fibrosis or Spinal Muscular Atrophy.
How is the sample collected?
LuckyGeneMDx uses non-invasive collection methods. You can provide a small saliva sample or a standard blood draw at one of our partner clinics. Our home collection kits use professional-grade stabilizing buffers to ensure DNA integrity during transit.
How accurate are the MDx results?
Our molecular diagnostic (MDx) testing utilizes Next-Generation Sequencing (NGS) with 99.9% clinical sensitivity for the variants we screen. However, no genetic test can detect 100% of all possible mutations. This is referred to as "Residual Risk."
What if I test positive as a carrier?
Being a carrier usually does not affect your own health. However, if your partner is also a carrier for the same condition, there is a 25% chance (1 in 4) that your child could be affected. We recommend discussing results with a board-certified genetic counselor.
Who has access to my genetic data?
Under HIPAA regulations, your data is only accessible to you, the laboratory clinical team, and your ordering physician. LuckyGeneMDx does not sell your data to pharmaceutical companies or insurance providers.