Carrier Screening Test

Phenome Longevity Verified independent store

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Many people carry genetic variants without ever experiencing symptoms themselves. These changes, however, can be passed on to children and may lead to inherited conditions if both parents carry mutations in the same gene. The Phenome Longevity Carrier Screening Test uses advanced genomic sequencing to analyse thousands of genes linked to serious inherited disorders. By identifying whether you or your partner carry specific genetic variants, the test empowers you to make informed and proactive reproductive decisions. Our comprehensive panel includes the most clinically relevant and widely recognised conditions, such as: Cystic Fibrosis (CFTR) Spinal Muscular Atrophy (SMN1) Sickle Cell Anaemia (HBB) Tay-Sachs Disease (HEXA) Fragile X Syndrome (FMR1) Show more