Basic

Username

2Lovebirds
Sex

Female
Current Location (City, State)

94523
Birthplace (City, State)

Oakland
Birthdate

February 2, 1989
Clinic/Bank/University/Doctor (USE COMMA BETWEEN MULTIPLE; SPELL FULL NAMES)

Xytex
Donor ID (Alphanumeric Value ONLY! - NO EXTRA INFORMATION - Separate Multiple ID's with ',' - or 'N/A', 'Unknown', 'Anonymous')

4898
Known 'Donor' Information (or 'None')

Year of Birth:1990Marital Status:SingleNumber of Children:0Religion:AgnosticOccupation:Personal TrainerBlood Type:B +Nationality: Maternal: Syrian, Israeli, Paternal: Russian, Polish Race:White Or CaucasianCMV Status:NEGLast Medical History Update:04/17/2018
I am a

Parent of Donor Conceived Person
Searching For

Sperm Donor, Half-Siblings, Full-Siblings, Donor Relatives
Known Genetic Health History (or 'None')

Beta-Thalassemia (HBB)No disease-causing mutations detected; normal complete blood count
Bloom Syndrome (BLM)No disease-causing mutations detected
Canavan Disease (ASPA)No disease-causing mutations detected
Chromosomal AnalysisNormal male karyotype
Cystic Fibrosis (CFTR)No disease-causing mutations detected
Familial Dysautonomia (IKBKAP)No disease-causing mutations detected
Familial Hyperinsulinism, ABCC8-Related (ABCC8)No disease-causing mutations detected
Fanconi Anemia Group C (FANCC)No disease-causing mutations detected
Gaucher Disease (GBA)No disease-causing mutations detected
Glycogen Storage Disease Type Ia (G6PC)No disease-causing mutations detected
Joubert Syndrome 2 (TMEM216)No disease-causing mutations detected
Maple Syrup Urine Disease Type 1B (BCKDHB)No disease-causing mutations detected
Maple Syrup Urine Disease Type 3 (DLD) also known as Dihydrolipoamide Dehydrogenase DeficiencyNo disease-causing mutations detected
Mucolipidosis Type IV (MCOLN1)No disease-causing mutations detected
Nemaline Myopathy, NEB-Related (NEB)No disease-causing mutations detected
Niemann-Pick Disease Type A (SMPD1)No disease-causing mutations detected
Niemann-Pick Disease Type B (SMPD1)No disease-causing mutations detected
Sickle Cell Disease (HBB)No disease-causing mutations detected; normal complete blood count
Spinal Muscular Atrophy (SMN1)No disease-causing mutations detected (exon 7 deletion not detected)
Tay-Sachs Disease (HEXA)No disease-causing mutations detected
Usher Syndrome Type IF (PCDH15)No disease-causing mutations detected
Usher Syndrome Type III (CLRN1)No disease-causing mutations detected
Age Discovered Donor Conception or Told Offspring

18
Social Parent(s) Type

Lesbian Couple
Month & Year I 'Donated' or Conceived (Parent or Offspring)

06/2018
Number of Naturally (non-DCP) Conceived Children ('zero' if none)

zero
Number of 'Donor' Children ('zero' if none)

zero
Number of Known 'Donor' Siblings ('zero' if none)

zero
Registry Memberships

I do not belong to any registries.
DNA Database Memberships

I still need to buy DNA memberships to the 3 big databases through the links on the Resources page
Paternal Haplogroup (or 'Unknown')

unknown
Maternal Haplogroup (or 'Unknown')

unknown
I MADE A MATCH!

Not Yet