James Peterson
Your Reports Summary
This is an overview of your 23andMe reports. It provides brief descriptions of your results but does not provide detailed information that may be important for understanding your results. 23andMe reports do not include all possible variants or account for other factors related to these conditions and traits.
Log into your 23andMe account for more details about each of your results. If you have concerns about your results, talk to a healthcare professional.
Your Reports Highlights
Certain results are highlighted because they may be unique or contain important information relevant to your health. The reports in your 23andMe account can provide more details about each of these results.
Carrier Status Reports0 highlighted of 41 reports
Wellness Reports2 highlighted of 8 reports
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●Lactose Intolerance Likely tolerant
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●Saturated Fat and Weight Likely similar weight
Ancestry Reports1 highlighted of 3 reports
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●Ancestry Composition 45.9% British & Irish
9 populations
Traits Reports3 highlighted of 22 reports
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●Asparagus Odor Detection 75% chance can smell, 25% chance can't smell
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●Bitter Taste 56% chance can taste, 44% chance can't taste
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●Sweet Taste 71% chance prefers salty, 29% chance prefers sweet
Ancestry Reports 1 highlighted report of 3 reports available
These reports let you explore what your DNA says about your origins and ancient ancestors.
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●Ancestry Composition
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European99.4%
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Northwestern European95.9%
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British & Irish45.9%
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French & German16.3%
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Scandinavian6.7%
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Broadly Northwestern European27.0%
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Southern European1.6%
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Broadly Southern European1.6%
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Broadly European1.8%
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East Asian & Native American0.6%
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Native American0.5%
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East Asian0.1%
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YakutLess than 0.1%
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Broadly East AsianLess than 0.1%
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Haplogroups
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MaternalK2a2
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PaternalG-L30
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Neanderthal AncestryMore Neanderthal variants than 59% of customers
Wellness Reports 2 highlighted reports of 8 reports available
These reports help you understand how your DNA influences your body's response to environmental factors like diet or lifestyle. Consider talking to a healthcare professional before making any major lifestyle changes or if you have any concerns about your results.
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Alcohol Flush ReactionUnlikely to flush
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Caffeine ConsumptionLikely consumes more
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Deep SleepNot determined
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Genetic WeightPredisposed to weigh about average
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Likely tolerant●Lactose Intolerance
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Muscle CompositionLikely sprinter
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Likely similar weight●Saturated Fat and Weight
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Sleep MovementLikely more movement during sleep
Traits Reports 3 highlighted reports of 22 reports available
These reports are a fun way to learn about how your DNA influences your physical appearance, preferences, and physical responses. The predictions are based on current knowledge of how genetic factors influence our traits.
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75% chance can smell, 25% chance can't smell●Asparagus Odor Detection
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Back Hair29% chance a lot of upper back hair, 71% chance little upper back hair
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Bald Spot67% chance no bald spot, 33% chance bald spot
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56% chance can taste, 44% chance can't taste●Bitter Taste
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Cheek Dimples70% chance no dimples, 30% chance dimples
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Cleft Chin75% chance no cleft chin, 25% chance cleft chin
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Earlobe Type18% chance attached earlobes, 82% chance detached earlobes
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Earwax Type90% chance wet earwax, 10% chance dry earwax
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Eye Color35% chance lighter eyes, 65% chance darker eyes
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Lighter eyes35%
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Blue3%
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Greenish blue3%
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Green9%
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Light hazel20%
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Darker eyes65%
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Dark hazel25%
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Light brown13%
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Dark brown27%
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Finger Length Ratio23% chance index finger longer, 77% chance ring finger longer
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Freckles45% chance a lot of freckles, 55% chance little freckling
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Hair Curliness7% chance curly, 93% chance straight or wavy
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Curly7%
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Big curls5%
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Small curls2%
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Very tight curls< 1%
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Straight or wavy93%
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Wavy15%
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Slightly wavy43%
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Straight35%
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Light or Dark Hair83% chance dark, 17% chance light
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Dark83%
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Black16%
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Dark brown67%
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Light17%
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Light brown15%
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Dark blond2%
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Light blond< 1%
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Male Hair Loss30% chance no hair loss, 70% chance hair loss
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Newborn Hair Amount40% chance lots of baby hair, 60% chance little baby hair
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Photic Sneeze Reflex12% chance photic sneeze reflex, 88% chance no photic sneeze reflex
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Red Hair1% chance red hair, 99% chance no red hair
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Skin Pigmentation96% chance lighter skin, 4% chance darker skin
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Lighter skin96%
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Very fair39%
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Moderately fair32%
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Light beige25%
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Darker skin4%
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Olive3%
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Light brown1%
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Dark brown< 1%
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71% chance prefers salty, 29% chance prefers sweet●Sweet Taste
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Toe Length Ratio47% chance big toe longer, 53% chance second toe longer
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Unibrow94% chance little or no unibrow, 6% chance moderate to thick unibrow
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Little or no unibrow94%
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No unibrow59%
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Little unibrow35%
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Moderate to thick unibrow6%
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Moderate to thick unibrow6%
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Widow's Peak76% chance no widow's peak, 24% chance widow's peak
Carrier Status Reports 0 highlighted reports of 41 reports available
These reports tell you about variants that may not affect your health, but could affect the health of your future family. For the conditions included in these reports, a person can be a carrier even if they don't have a personal or family history of the disease. Consider talking to a healthcare professional before making any major lifestyle changes or if you have any concerns about your results.
If you see "Variant not detected" for a Carrier Status report, it means you're not a carrier of the tested variant(s). Keep in mind that while our Carrier Status reports cover many variants, they don't include all possible variants associated with each condition. So it's still possible to be a carrier of a variant not included in our test. Learn more.
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ARSACSVariant not detected
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Agenesis of the Corpus Callosum with Peripheral NeuropathyVariant not detected
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Autosomal Recessive Polycystic Kidney DiseaseVariant not detected
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Beta Thalassemia and Related HemoglobinopathiesVariant not detected
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Bloom SyndromeVariant not detected
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Canavan DiseaseVariant not detected
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Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)Variant not detected
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Cystic FibrosisVariant not detected
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D-Bifunctional Protein DeficiencyVariant not detected
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Dihydrolipoamide Dehydrogenase DeficiencyVariant not detected
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Familial DysautonomiaVariant not detected
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Fanconi Anemia Group CVariant not detected
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GRACILE SyndromeVariant not detected
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Glycogen Storage Disease Type IaVariant not detected
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Glycogen Storage Disease Type IbVariant not detected
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Hereditary Fructose IntoleranceVariant not detected
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Herlitz Junctional Epidermolysis Bullosa (LAMB3-Related)Variant not detected
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Leigh Syndrome, French Canadian TypeVariant not detected
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Limb-Girdle Muscular Dystrophy Type 2DVariant not detected
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Limb-Girdle Muscular Dystrophy Type 2EVariant not detected
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Limb-Girdle Muscular Dystrophy Type 2IVariant not detected
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MCAD DeficiencyVariant not detected
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Maple Syrup Urine Disease Type 1BVariant not detected
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Mucolipidosis Type IVVariant not detected
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Neuronal Ceroid Lipofuscinosis (CLN5-Related)Variant not detected
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Neuronal Ceroid Lipofuscinosis (PPT1-Related)Variant not detected
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Niemann-Pick Disease Type AVariant not detected
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Nijmegen Breakage SyndromeVariant not detected
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Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)Variant not detected
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Pendred Syndrome and DFNB4 Hearing LossVariant not detected
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Phenylketonuria and Related DisordersVariant not detected
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Primary Hyperoxaluria Type 2Variant not detected
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Rhizomelic Chondrodysplasia Punctata Type 1Variant not detected
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Salla DiseaseVariant not detected
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Sickle Cell AnemiaVariant not detected
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Sjögren-Larsson SyndromeVariant not detected
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Tay-Sachs DiseaseVariant not detected
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Tyrosinemia Type IVariant not detected
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Usher Syndrome Type 1FVariant not detected
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Usher Syndrome Type 3AVariant not detected
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Zellweger Syndrome Spectrum (PEX1-Related)Variant not detected