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Does anyone know if it is standard for clinics - in the Donor genetic pre screen- to test for Fragile X? Does anyone know which genetic mutations are most commonly tested for- in the pre screen?

All the clinics I have cycled with required a chromosomal analysis (which did test for fragile X) and a screen for cystic fibrosis. Once I had this completed for my first donation, the other clinics I worked with allowed me to use these records rather then be retested. If you have more questions I can look up my chromosomal analysis and see exactly what it said.