This donor is a healthy carrier for a genetic disease.
Please see his Genetic Testing Summary and Acknowledgment of Genetic Risk for details

Physical

Height:
6'1"
(185 cm)
Weight:
220 lb
(99 kg)
Eye Color:
Green
Hair:
Brown/
Curly
Skin Tone:
Medium Light
Ancestry:
Caucasian
Blood Type:
A+
Ethnic Background:
English-Swedish/Polish
Education:
Pursuing BA/Finance
Occupation:
Student
Interests:
Beatboxing, Hiking, Swimming, Writing

Medical

Question Response
Have you or any of your family members been diagnosed with alcoholism or drug addiction?
If yes, relation and age affected:
No
Any dietary restrictions?
If yes, explain:
No
Do you wear glasses or contact lenses?
Are you near or far-sighted?
No
Allergies (medicines, food, pollens)?
If yes, please list substance and reaction caused:
Yes - Pollen, seasonal, watery eyes, sneezing, nasal congestion
CMV IgG AntibodyNegative
CMV IgM AntibodyNegative
Note any comments regarding above items:N/A

Family Medical History
See list of questions asked here

Question Response
Current age or age at death 57
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Incontinence
40
Medication
Question Response
Current age or age at death 56
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Knee surgery
56
highly active
Question Response
Current age or age at death 26
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 84
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 85
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 64
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 54
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 62
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 43
Living / DeadDead
Cause of death and any treatment prior to deathHeart Attack
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Heart attack
43
Treatment (unknown) before passing
Question Response
Current age or age at death 45
Living / DeadDead
Cause of death and any treatment prior to deathPneumonia
Health Problems
Disease
Age Diagnosed
Treatment For Condition
Pneumonia
45
Hospitalization
Question Response
Current age or age at death 61
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 59
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy
Question Response
Current age or age at death 64
Living / DeadLiving
Cause of death and any treatment prior to deathN/A
Health Problems
Healthy

Religion:

Faith None
Denomination Agnostic

Updates to Profile

Update AvailableYes
Updates - PersonalUpdate received September 2025: Occupation has changed to Investment Analyst; Donor has obtained certificates in Risk Management and Wealth Management.
Updates - MedicalUpdate received September 2025: Donor underwent a thyroid lobectomy at age 23 to remove a benign nodule.UPDATE Jan 2026: Donor 6248 has been found to be a carrier of a gene change (5T;TG11) in the CFTR gene. The variant this donor carries is considered to be low risk, which means it is highly unlikely to cause disease if the recipient (egg source) is also a carrier of a variant in the CFTR gene and both variants are passed onto a child. Changes in the CFTR gene have been associated with cystic fibrosis (CF) and CFTR-related disorders (CFTR-RD). No child with these conditions has been reported, rather the donor’s CFTR carrier status was discovered on a special testing request from a client who is a known carrier. The donor had his original genetic testing in 2019, which did not report this variant unless another CFTR variant (specifically R117H) was identified. As the donor does not have the R117H variant, the original testing lab did not report he carried the 5T;TG11 variant.
Updates - Family Medical HistoryUpdate received September 2025: Donor's Father was diagnosed with thyroid disease at age 50, treated with Levothyroxine.UPDATE Feb 2026: A client reports that her child was born with a cleft lip, ptosis, and a coloboma of his upper eyelid (right). No additional infomation is available regarding this report at this time. The donor has been placed in Investigation until more information becomes available. No other donor conceived pregnancies/children have been reported to have medical issues.UPDATE Feb 2026: In addition to the information above, the client reports that her child was born with a sacral dimple. Per the client, several ultrasounds were conducted during her pregnancy with no abnormal findings. Imaging studies have included ultrasounds of her child’s head, chest, back and abdomen, an MRI of his face and head, and an x-ray of his abdomen and back. All imaging, per the client’s report, has been normal. Surgery to repair the child’s cleft lip is scheduled.The client reports that she has been encouraged by their ENT, ophthalmologist, and oculoplastic surgeon to pursue genetic testing but has yet to receive an official referral. As such, no genetic testing has been conducted at this time.She denies any history of such findings in her personal or family history. This child’s medical issues can be isolated findings or related to a genetic condition, a chromosome anomaly, or an environmental cause. When we see two or more findings in different organ systems, the suspicion for a chromosome abnormality or genetic syndrome is increased. Without knowing the underlying cause for these medical issues, we are unable to assess the risk for recurrence in other donor-conceived children.If all the medical issues were isolated, the recurrence risk for one would be independent of the others. If they were caused by one underlying genetic etiology, the recurrence would depend on the inheritance pattern of that condition. If the etiologywas environmental, the risk for recurrence would not be expected to be increased above the general population risk.UPDATE March 2026: Following the completion of the investigation process, it is believed that this is most likely a sporadic occurrence with a low risk of recurrence in other donor-conceived children; however, as the cause of these conditions remains unknown, we cannot offer a specific risk for recurrence.