2/5/25, 12:05 PM Vasilios Syrros Reports Summary - 23andMe Your genetic results were analyzed on a previous version of our genotyping platform. Click here for more information. [https://permalinks.23andme.com/pdf/PN-20-0312.pdf] Vasilios Syrros Reports Summary 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. Health Predisposition Reports 9+ reports available Genetic factors that may influence your chances of developing certain health conditions. Consider talking to a healthcare professional if you have a personal or family history of one of these conditions or have concerns about your results. Our reports do not include all possible genetic variants that could affect these conditions. Other factors can also affect your risk of developing these conditions, including lifestyle, environment, and family history. Age-Related Macular Degeneration Celiac Disease Hereditary Hemochromatosis (HFE‑Related) Increased risk Slightly increased risk Variant detected, not likely at increased risk Alpha-1 Antitrypsin Deficiency Variants not detected BRCA1/BRCA2 (Selected Variants) Variants not detected G6PD Deficiency Variants not detected Hereditary Thrombophilia Variants not detected Late-Onset Alzheimer's Disease Variant not detected Parkinson's Disease Variants not detected https://you.23andme.com/reports/print/ 1/6 2/5/25, 12:05 PM Carrier Status Reports Vasilios Syrros Reports Summary - 23andMe 43+ reports available Learn whether you have specific genetic variants that may not affect your health, but could affect your children's health. 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. 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 Familial Hyperinsulinism (ABCC8-Related) Variant not detected Fanconi Anemia Group C Variant not detected GRACILE Syndrome Variant not detected Gaucher Disease Type 1 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 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 https://you.23andme.com/reports/print/ 2/6 2/5/25, 12:05 PM Vasilios Syrros Reports Summary - 23andMe Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related) Variant not detected Pendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related) 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 Severe Junctional Epidermolysis Bullosa (LAMB3-Related) 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 Spectrum Disorder (PEX1-Related) Variant not detected Wellness Reports 8+ reports available Find out how your DNA may affect your body's response to diet, exercise, and sleep. 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 to consume more Deep Sleep Genetic Weight Less likely to be a deep sleeper Predisposed to weigh about average Lactose Intolerance Likely intolerant Muscle Composition Common in elite power athletes Saturated Fat and Weight Sleep Movement https://you.23andme.com/reports/print/ Likely similar weight Likely more than average movement 3/6 2/5/25, 12:05 PM Vasilios Syrros Reports Summary - 23andMe Ancestry Reports 4+ reports available Discover the story of your ancient ancestors, your origins, and your ancestral background. Ancestry Composition European 99.8% Southern European 99.8% Greek & Balkan 82.0% Italian 17.5% Broadly Southern European 0.3% Western Asian & North African 0.2% North African 0.2% Maternal Haplogroup U1a1 Neanderthal Ancestry Fewer Neanderthal variants than 60% of customers Paternal Haplogroup E-M78 https://you.23andme.com/reports/print/ 4/6 2/5/25, 12:05 PM Traits Reports Vasilios Syrros Reports Summary - 23andMe 33+ reports available Explore the genetics behind your appearance and senses. Ability to Match Musical Pitch Asparagus Odor Detection About a 50/50 chance of being able to match a musical pitch Likely can smell Back Hair Likely little upper back hair Bald Spot Likely no bald spot Bitter Taste Cheek Dimples Cilantro Taste Aversion Cleft Chin Likely can taste Likely no dimples Slightly higher odds of disliking cilantro Likely no cleft chin Dandruff Less likely to get dandruff Earlobe Type Likely detached earlobes Early Hair Loss Likely no hair loss Earwax Type Likely wet earwax Eye Color Fear of Heights Finger Length Ratio Freckles Hair Photobleaching Hair Texture Hair Thickness Light or Dark Hair Misophonia Mosquito Bite Frequency Motion Sickness Newborn Hair Photic Sneeze Reflex Likely brown or hazel eyes Less likely than average to be afraid of heights Likely ring finger longer Likely little freckling About a 50/50 chance of experiencing hair photobleaching Likely straight or wavy Less likely to have thick hair Likely dark Average odds of hating chewing sounds Likely bitten as often as others About a 50/50 chance of experiencing motion sickness Likely little baby hair Likely no photic sneeze reflex Red Hair Likely no red hair Skin Pigmentation Likely lighter skin Stretch Marks Less likely to have stretch marks Sweet vs. Salty Likely prefers salty Toe Length Ratio Unibrow Wake-Up Time https://you.23andme.com/reports/print/ Likely second toe longer Likely at least a little unibrow Likely to wake up around 7:09 am 5/6 2/5/25, 12:05 PM Vasilios Syrros Reports Summary - 23andMe Widow's Peak Likely no widow's peak Vasilios Syrros's Reports Summary, printed on 2025-02-05 UTC © 2025 23andMe, Inc. 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