Genetic carriers a person
GenoLife
Delivery time
No especificado
Sample
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It is a genetic test performed on healthy people to detect their risk of transmitting a series of recessive genetic diseases to their children. To do this, a series of genes responsible for these diseases are studied. Any healthy person with no family history may have a defective one of the two copies we all have for each gene.
Serious and prevalent disorders seen in all ethnic groups. Improved spinal muscular atrophy screening helps identify silent carriers.
•Comprehensive analysis of fragile X syndrome, including AGG disruptions
•Complete gene sequencing with deletion and duplication analysis, with a 99% detection rate for most genes. Includes all disorders recommended by ACOG (American College of Obstetricians and Gynecologists) and ACMG (American College of Medical Genetics and Genomics). 288 genes analyzed. 21 X-linked disorders.
Other tests
VitaLIFE Genetic: 41 SNPs associated with deficiencies
201,60€
VenuLife + Thrombopanel + Polycystic Ovary Syndrome
264,00€
MTHFR variants
108,00€