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

  • Lactose Intolerance
    Likely tolerant
  • Saturated Fat and Weight
    Likely similar weight

Ancestry Reports1 highlighted of 3 reports

  • Ancestry Composition
    45.9% British & Irish
    9 populations

Traits Reports3 highlighted of 22 reports

  • Asparagus Odor Detection
    75% chance can smell, 25% chance can't smell
  • Bitter Taste
    56% chance can taste, 44% chance can't taste
  • 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.

  • Ancestry Composition
    • European
      99.4%
      • Northwestern European
        95.9%
        • British & Irish
          45.9%
        • French & German
          16.3%
        • Scandinavian
          6.7%
        • Broadly Northwestern European
          27.0%
      • Southern European
        1.6%
        • Broadly Southern European
          1.6%
      • Broadly European
        1.8%
    • East Asian & Native American
      0.6%
      • Native American
        0.5%
      • East Asian
        0.1%
        • Yakut
          Less than 0.1%
        • Broadly East Asian
          Less than 0.1%
  • Haplogroups
    • Maternal
      K2a2
    • Paternal
      G-L30
  • Neanderthal Ancestry
    More 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.

  • Alcohol Flush Reaction
    Unlikely to flush
  • Caffeine Consumption
    Likely consumes more
  • Deep Sleep
    Not determined
  • Genetic Weight
    Predisposed to weigh about average
  • Lactose Intolerance
    Likely tolerant
  • Muscle Composition
    Likely sprinter
  • Saturated Fat and Weight
    Likely similar weight
  • Sleep Movement
    Likely 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.

  • Asparagus Odor Detection
    75% chance can smell, 25% chance can't smell
  • Back Hair
    29% chance a lot of upper back hair, 71% chance little upper back hair
  • Bald Spot
    67% chance no bald spot, 33% chance bald spot
  • Bitter Taste
    56% chance can taste, 44% chance can't taste
  • Cheek Dimples
    70% chance no dimples, 30% chance dimples
  • Cleft Chin
    75% chance no cleft chin, 25% chance cleft chin
  • Earlobe Type
    18% chance attached earlobes, 82% chance detached earlobes
  • Earwax Type
    90% chance wet earwax, 10% chance dry earwax
  • Eye Color
    35% chance lighter eyes, 65% chance darker eyes
    • Lighter eyes
      35%
      • Blue
        3%
      • Greenish blue
        3%
      • Green
        9%
      • Light hazel
        20%
    • Darker eyes
      65%
      • Dark hazel
        25%
      • Light brown
        13%
      • Dark brown
        27%
  • Finger Length Ratio
    23% chance index finger longer, 77% chance ring finger longer
  • Freckles
    45% chance a lot of freckles, 55% chance little freckling
  • Hair Curliness
    7% chance curly, 93% chance straight or wavy
    • Curly
      7%
      • Big curls
        5%
      • Small curls
        2%
      • Very tight curls
        < 1%
    • Straight or wavy
      93%
      • Wavy
        15%
      • Slightly wavy
        43%
      • Straight
        35%
  • Light or Dark Hair
    83% chance dark, 17% chance light
    • Dark
      83%
      • Black
        16%
      • Dark brown
        67%
    • Light
      17%
      • Light brown
        15%
      • Dark blond
        2%
      • Light blond
        < 1%
  • Male Hair Loss
    30% chance no hair loss, 70% chance hair loss
  • Newborn Hair Amount
    40% chance lots of baby hair, 60% chance little baby hair
  • Photic Sneeze Reflex
    12% chance photic sneeze reflex, 88% chance no photic sneeze reflex
  • Red Hair
    1% chance red hair, 99% chance no red hair
  • Skin Pigmentation
    96% chance lighter skin, 4% chance darker skin
    • Lighter skin
      96%
      • Very fair
        39%
      • Moderately fair
        32%
      • Light beige
        25%
    • Darker skin
      4%
      • Olive
        3%
      • Light brown
        1%
      • Dark brown
        < 1%
  • Sweet Taste
    71% chance prefers salty, 29% chance prefers sweet
  • Toe Length Ratio
    47% chance big toe longer, 53% chance second toe longer
  • Unibrow
    94% chance little or no unibrow, 6% chance moderate to thick unibrow
    • Little or no unibrow
      94%
      • No unibrow
        59%
      • Little unibrow
        35%
    • Moderate to thick unibrow
      6%
      • Moderate to thick unibrow
        6%
  • Widow's Peak
    76% 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.

  • ARSACS
    Variant not detected
  • Agenesis of the Corpus Callosum with Peripheral Neuropathy
    Variant not detected
  • Autosomal Recessive Polycystic Kidney Disease
    Variant not detected
  • Beta Thalassemia and Related Hemoglobinopathies
    Variant not detected
  • Bloom Syndrome
    Variant not detected
  • Canavan Disease
    Variant not detected
  • Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)
    Variant not detected
  • Cystic Fibrosis
    Variant not detected
  • D-Bifunctional Protein Deficiency
    Variant not detected
  • Dihydrolipoamide Dehydrogenase Deficiency
    Variant not detected
  • Familial Dysautonomia
    Variant not detected
  • Fanconi Anemia Group C
    Variant not detected
  • GRACILE Syndrome
    Variant not detected
  • Glycogen Storage Disease Type Ia
    Variant not detected
  • Glycogen Storage Disease Type Ib
    Variant not detected
  • Hereditary Fructose Intolerance
    Variant not detected
  • Herlitz Junctional Epidermolysis Bullosa (LAMB3-Related)
    Variant not detected
  • Leigh Syndrome, French Canadian Type
    Variant not detected
  • Limb-Girdle Muscular Dystrophy Type 2D
    Variant not detected
  • Limb-Girdle Muscular Dystrophy Type 2E
    Variant not detected
  • Limb-Girdle Muscular Dystrophy Type 2I
    Variant not detected
  • MCAD Deficiency
    Variant not detected
  • Maple Syrup Urine Disease Type 1B
    Variant not detected
  • Mucolipidosis Type IV
    Variant not detected
  • Neuronal Ceroid Lipofuscinosis (CLN5-Related)
    Variant not detected
  • Neuronal Ceroid Lipofuscinosis (PPT1-Related)
    Variant not detected
  • Niemann-Pick Disease Type A
    Variant not detected
  • Nijmegen Breakage Syndrome
    Variant not detected
  • Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)
    Variant not detected
  • Pendred Syndrome and DFNB4 Hearing Loss
    Variant not detected
  • Phenylketonuria and Related Disorders
    Variant not detected
  • Primary Hyperoxaluria Type 2
    Variant not detected
  • Rhizomelic Chondrodysplasia Punctata Type 1
    Variant not detected
  • Salla Disease
    Variant not detected
  • Sickle Cell Anemia
    Variant not detected
  • Sjögren-Larsson Syndrome
    Variant not detected
  • Tay-Sachs Disease
    Variant not detected
  • Tyrosinemia Type I
    Variant not detected
  • Usher Syndrome Type 1F
    Variant not detected
  • Usher Syndrome Type 3A
    Variant not detected
  • Zellweger Syndrome Spectrum (PEX1-Related)
    Variant not detected