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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

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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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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

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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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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

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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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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

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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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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

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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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