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All carrier status reports

Report Gene Variants Relevant Ethnicities

ARSACS SACS 1 Variant French Canadian
Agenesis of the Corpus Callosum with Peripheral Neuropathy SLC12A6 1 Variant French Canadian
Autosomal Recessive Polycystic Kidney Disease PKHD1 3 Variants N/A
Beta Thalassemia and Related Hemoglobinopathies HBB 10 Variants Cypriot, Greek, Italian, Sardinian
Bloom Syndrome BLM 1 Variant Ashkenazi Jewish
Congenital Disorder of Glycosylation Type 1a (PMM2-CDG) PMM2 2 Variants Danish
Cystic Fibrosis CFTR 28 Variants European, Hispanic/Latino, Ashkenazi Jewish
D-Bifunctional Protein Deficiency HSD17B4 2 Variants N/A
Dihydrolipoamide Dehydrogenase Deficiency DLD 1 Variant Ashkenazi Jewish
Familial Dysautonomia IKBKAP 1 Variant Ashkenazi Jewish
Fanconi Anemia Group C FANCC 3 Variants Ashkenazi Jewish
GRACILE Syndrome BCS1L 1 Variant Finnish
Glycogen Storage Disease Type Ia G6PC 1 Variant Ashkenazi Jewish
Glycogen Storage Disease Type Ib SLC37A4 2 Variants N/A
Hereditary Fructose Intolerance ALDOB 3 Variants European
Leigh Syndrome, French Canadian Type LRPPRC 1 Variant French Canadian
Limb-Girdle Muscular Dystrophy Type 2D SGCA 1 Variant Finnish
Limb-Girdle Muscular Dystrophy Type 2E SGCB 1 Variant Southern Indiana Amish
Limb-Girdle Muscular Dystrophy Type 2I FKRP 1 Variant European
MCAD Deficiency ACADM 3 Variants Northern European
Maple Syrup Urine Disease Type 1B BCKDHB 2 Variants Ashkenazi Jewish
Neuronal Ceroid Lipofuscinosis (CLN5-Related) CLN5 1 Variant Finnish
Neuronal Ceroid Lipofuscinosis (PPT1-Related) PPT1 3 Variants Finnish
Niemann-Pick Disease Type A SMPD1 3 Variants Ashkenazi Jewish
Nijmegen Breakage Syndrome NBN 1 Variant Eastern European
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related) GJB2 2 Variants Ashkenazi Jewish, European
Pendred Syndrome and DFNB4 Hearing Loss SLC26A4 6 Variants N/A
Primary Hyperoxaluria Type 2 GRHPR 1 Variant European
Rhizomelic Chondrodysplasia Punctata Type 1 PEX7 1 Variant N/A
Sickle Cell Anemia HBB 1 Variant African
Sjögren-Larsson Syndrome ALDH3A2 1 Variant Swedish
Tay-Sachs Disease HEXA 4 Variants Ashkenazi Jewish, Cajun
Tyrosinemia Type I FAH 4 Variants French Canadian, Finnish
Usher Syndrome Type 1F PCDH15 1 Variant Ashkenazi Jewish
Usher Syndrome Type 3A CLRN1 1 Variant Ashkenazi Jewish
Zellweger Syndrome Spectrum (PEX1-Related) PEX1 1 Variant N/A

*Our tests can be used to determine carrier status in adults from saliva collected using an FDA-cleared collection device (Oragene·DX model OGD-500.001), but cannot determine if you have two copies of the genetic variant. The tests are not intended to diagnose a disease, or tell you anything about your risk for developing a disease in the future. On their own, carrier status tests are not intended to tell you anything about the health of your fetus, or your newborn child's risk of developing a particular disease later in life.

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All traits reports

Asparagus Odor Detection
Back Hair (available for men only)
Bald Spot (available for men only)
Bitter Taste Perception
Cheek Dimples
Cleft Chin
Earlobe Type
Earwax Type
Eye Color
Finger Length Ratio
Freckles
Hair Curliness
Light or Dark Hair
Male Hair Loss (available for men only)
Newborn Hair Amount
Photic Sneeze Reflex
Red Hair
Skin Pigmentation
Sweet Taste Preference
Toe Length Ratio
Unibrow
Widow's Peak