ADDITIONAL AFFECTED SIBLING FOR TRIO REQUISITION 2025

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  1. Click ‘Get Form’ to open the ADDITIONAL AFFECTED SIBLING FOR TRIO REQUISITION in the editor.
  2. Begin by filling out the 'Patient Information' section. Enter the patient's last name, first name, middle initial, date of birth, and biological sex. Ensure all fields are completed accurately.
  3. In the 'Reporting Recipients' section, provide details for the ordering physician and institution. Include their email and phone number for seamless communication.
  4. Proceed to the 'Payment' section. Choose between self-payment or institutional billing options and fill in necessary details accordingly.
  5. Complete the 'Indication for Testing' section by providing clinical information regarding the patient. This includes any relevant ICD-10 diagnosis codes and a brief medical history.
  6. Finally, review your entries for accuracy before signing at the bottom of the form. Ensure that all required signatures are obtained from both parents if applicable.

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If you have a sibling, they received their own uniquely shuffled set of chromosomes, and theres no guarantee they got the same genes from either parent that you did. You each got ~50% of each parents genes, shuffled more or less at random, and the amount of DNA you share from each parent is roughly 50%*50% or 25%.
For example, if you share 50% of your DNA with someone in your generation, that means you are full siblings, i.e., descended from the same parents. If you share 12.5%, that likely means you are first cousins, i.e., you share one pair of grandparents.
Trio testing is when the patients genome or exome is compared with sequences obtained from both of their biological parents. This is because if neither parent has their childs disease, it can be reasonably assumed that the variants found in the parents genomes are not the cause of their childs condition.
The differences in genetic code between siblings are due to variations in the chromosomes passed down to them from their parents. This, more often than skeletons in the closet, also explains why some siblings will receive different ethnicity or ancestry results.
The reason there is such a wide range of variation in the percentage of shared DNA among siblings is recombination: while both of them received all their DNA from the same two people, the exact 50% they inherited from each is random.