12/14/2015 Your Reports 23andMe
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Your Reports
Learn what your DNA says about you.
Click on the cards to view your detailed reports.
Showing all 65 reports
Category
All Reports
Carrier Status
Wellness
Traits
Ancestry
Status Variant
Present
Ancestry Composition
Ancestry
99.5% EuropeanThe analysis considers DNA you received from all of your ancestors worldwide on both sides of your family.
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Facial Features
Trait
6 ReportsOur resemblance to family members can be most obvious in our faces.
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Hair
Trait
6 ReportsYour DNA has a big influence on the color of your hair, your hair texture, and other hair traits.
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Physical Characteristics
Trait
4 ReportsGenes shape our bodies and influence many of our physical characteristics.
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Physical Responses
Trait
1 ReportHow you respond to your environment may have something to do with your genes.
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12/14/2015 Your Reports 23andMe
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Skin
Trait
2 ReportsThe skin is the largest organ of the body and how it looks is influenced by your genes.
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Taste and Smell
Trait
3 ReportsYour genes may help explain why you can smell certain things that other people can't, and why you prefer
certain tastes over others.
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Neanderthal Ancestry
Ancestry
>57% of UsersNeanderthals were ancient humans who interbred with modern humans before becoming extinct 40,000 years
ago. This report tells you how…
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Haplogroups
Ancestry
Maternal: H1 Paternal: I1
Haplogroups can tell you where a small portion of your ancestors originated thousands of years ago. Your
haplogroups can shed light on…
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Alcohol Flush Reaction
Wellness • ALDH2 gene
Unlikely to flushThe alcohol flush reaction is characterized by redness or flushing of the face or neck after consuming alcohol.
People who experience…
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Caffeine Consumption
Wellness • CYP1A2 and AHR genes
12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 3/10
Likely consumes lessCaffeine is the most widely consumed drug in the world. The amount of caffeine you consume - whether it's
from coffee, tea, or soft…
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Lactose Intolerance
Wellness • LCT gene
Likely tolerantDairy products like milk, yogurt, and cheese contain the sugar lactose. An enzyme called lactase breaks down
this sugar. If you don't…
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Muscle Composition
Wellness • ACTN3 gene
Likely sprinterOur muscles are made up of two main types of muscle fibers: "fast-twitch" and "slow-twitch." Exercise
performance may, in part, be due…
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ARSACS
Carrier Status • SACS gene
Variant not detectedARSACS is a rare genetic disorder characterized by loss of sensation and muscle control, as well as muscle
stiffness that worsens over…
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Agenesis of the Corpus Callosum with Peripheral Neuropathy
Carrier Status • SLC12A6 gene
Variant not detectedACCPN is a rare genetic disorder. It is characterized by an incomplete connection between the two sides of
the brain. This causes…
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Autosomal Recessive Polycystic Kidney Disease
Carrier Status • PKHD1 gene
Variant not detectedARPKD is a rare genetic disorder. It is characterized by kidney, liver, and lung problems as well as urinary tract
infections and high…
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12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 4/10
Beta Thalassemia and Related Hemoglobinopathies
Carrier Status • HBB gene
Variant not detectedBeta thalassemia is a genetic disorder characterized by anemia and fatigue as well as bone deformities and
organ problems. A person…
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Bloom Syndrome
Carrier Status • BLM gene
Variant not detectedBloom syndrome is a rare genetic disorder characterized by impaired growth and increased risk of infections
and cancer. A person must…
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Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
Carrier Status • PMM2 gene
Variant not detectedPMM2-CDG is a rare genetic disorder that affects the nervous system and other parts of the body. It is
characterized by developmental…
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Cystic Fibrosis
Carrier Status • CFTR gene
Variant not detectedCystic fibrosis is a rare genetic disorder characterized by impaired lung and digestive function. A person must
have two variants in…
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D-Bifunctional Protein Deficiency
Carrier Status • HSD17B4 gene
Variant not detectedDBPD is a rare genetic disorder. It is characterized by abnormal muscle tone, developmental disability,
seizures, and early death. A…
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Dihydrolipoamide Dehydrogenase Deficiency
Carrier Status • DLD gene
12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 5/10
Variant not detectedDLD deficiency is a rare genetic disorder. It is typically characterized by low muscle tone and episodes of brain
injury accompanied by…
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Familial Dysautonomia
Carrier Status • IKBKAP gene
Variant not detectedFamilial dysautonomia is a rare genetic disorder that affects many different parts of the body. It is
characterized by severe…
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Fanconi Anemia Group C
Carrier Status • FANCC gene
Variant not detectedFanconi anemia group C is a rare genetic disorder. It is characterized by a decreased production of blood
cells, birth defects, and an…
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GRACILE Syndrome
Carrier Status • BCS1L gene
Variant not detectedGRACILE syndrome is a rare genetic disorder. It is characterized by impaired growth before birth, iron buildup,
liver damage, and death…
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Glycogen Storage Disease Type Ia
Carrier Status • G6PC gene
Variant not detectedGSDIa is a rare genetic disorder. It is characterized by low blood sugar, liver and kidney problems, and poor
growth. A person must…
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Glycogen Storage Disease Type Ib
Carrier Status • SLC37A4 gene
Variant not detectedGSDIb is a rare genetic disorder. It is characterized by low blood sugar, liver and kidney problems, and
frequent infections. A person…
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12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 6/10
Hereditary Fructose Intolerance
Carrier Status • ALDOB gene
Variant not detectedHereditary fructose intolerance is a rare genetic disorder. It is characterized by low blood sugar levels,
stomach pain, and vomiting…
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Leigh Syndrome, French Canadian Type
Carrier Status • LRPPRC gene
Variant not detectedLSFC is a rare genetic disorder. It is characterized by life-threatening periods of lactic acid buildup and brain
injury as well as…
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Limb-Girdle Muscular Dystrophy Type 2D
Carrier Status • SGCA gene
Variant not detectedLGMD2D is a rare genetic disorder. It is characterized by muscle weakness that worsens over time as well as
heart and lung problems. A…
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Limb-Girdle Muscular Dystrophy Type 2E
Carrier Status • SGCB gene
Variant not detectedLGMD2E is a rare genetic disorder. It is characterized by muscle weakness that worsens over time as well as
heart and lung problems. A…
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Limb-Girdle Muscular Dystrophy Type 2I
Carrier Status • FKRP gene
Variant not detectedLGMD2I is a rare genetic disorder. It is characterized by muscle weakness that worsens over time as well as
heart and lung problems. A…
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MCAD Deficiency
Carrier Status • ACADM gene
12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 7/10
Variant not detectedMCAD deficiency is a rare genetic disorder characterized by episodes of very low blood sugar while fasting or
under stress. A person…
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Maple Syrup Urine Disease Type 1B
Carrier Status • BCKDHB gene
Variant not detectedMSUD 1B is a rare genetic disorder. It is characterized by poor growth and feeding, slowed mental and
physical processes, and urine…
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Neuronal Ceroid Lipofuscinosis (CLN5-Related)
Carrier Status • CLN5 gene
Variant not detectedCLN5-related NCL is a rare genetic disorder. It is characterized by seizures, vision loss, and intellectual
disability. A person must…
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Neuronal Ceroid Lipofuscinosis (PPT1-Related)
Carrier Status • PPT1 gene
Variant not detectedPPT1-related NCL is a rare genetic disorder. It is characterized by seizures, vision loss, and intellectual
disability. A person must…
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Niemann-Pick Disease Type A
Carrier Status • SMPD1 gene
Variant not detectedNiemann-Pick disease type A is a rare genetic disorder. It is characterized by an enlarged liver and spleen,
developmental disability…
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Nijmegen Breakage Syndrome
Carrier Status • NBN gene
Variant not detectedNijmegen breakage syndrome is a rare genetic disorder. It is characterized by developmental delay, recurring
infections, and an…
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12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 8/10
Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
Carrier Status • GJB2 gene
Variant not detectedDFNB1 is a type of inherited hearing loss that can be moderate to severe. Symptoms are typically noticed in
newborns. A person must…
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Pendred Syndrome and DFNB4 Hearing Loss
Carrier Status • SLC26A4 gene
Variant not detectedPendred syndrome and DFNB4 are genetic disorders characterized by deafness and structural problems with
the inner ear. Pendred syndrome…
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Primary Hyperoxaluria Type 2
Carrier Status • GRHPR gene
Variant not detectedPH2 is a rare genetic disorder. It is characterized by frequent kidney stones that can lead to kidney failure if left
untreated. A…
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Rhizomelic Chondrodysplasia Punctata Type 1
Carrier Status • PEX7 gene
Variant not detectedRCDP1 is a rare genetic disorder. It is characterized by bone abnormalities, cataracts, and intellectual
disability. A person must have…
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Sickle Cell Anemia
Carrier Status • HBB gene
Variant not detectedSickle cell anemia is a genetic disorder characterized by anemia, episodes of pain, and frequent infections. A
person must have two HbS…
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Sjögren-Larsson Syndrome
Carrier Status • ALDH3A2 gene
12/14/2015 Your Reports 23andMe
https://you.23andme.com/reports/ 9/10
Variant not detectedSjögren-Larsson syndrome is a rare genetic disorder. It is characterized by scaly dry skin, intellectual disability,
and persistent…
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Tay-Sachs Disease
Carrier Status • HEXA gene
Variant not detectedTay-Sachs disease is a rare genetic disorder. It is characterized by a loss of strength and coordination over time
as well as…
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Tyrosinemia Type I
Carrier Status • FAH gene
Variant not detectedTyrosinemia type I is a rare genetic disorder. It is characterized by high levels of the amino acid tyrosine that
can lead to liver and…
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Usher Syndrome Type 1F
Carrier Status • PCDH15 gene
Variant not detectedUsher 1F is a rare genetic disorder. It is characterized by deafness at birth, poor balance, and vision loss that
worsens over time. A…
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Usher Syndrome Type 3A
Carrier Status • CLRN1 gene
Variant not detectedUsher 3A is a rare genetic disorder. It is characterized by hearing and vision loss that begins in late childhood
and worsens over…
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Zellweger Syndrome Spectrum (PEX1-Related)
Carrier Status • PEX1 gene
Variant not detectedZSS is a group of rare genetic disorders. The form of ZSS covered by this report is characterized by impaired
hearing, vision, and…
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12/14/2015 Your Reports 23andMe
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