We will not share your genetic data with employers, insurance companies, public databases or 3rd party marketers without your explicit consent. We will not release any individual-level personal information to law enforcement unless we are required to do so by court order, subpoena, search warrant or other requests that we determine are legally valid. https://www.23andme.com/privacy/
We will not share your genetic data with employers, insurance companies, public databases or 3rd party marketers without your explicit consent. We will not release any individual-level personal information to law enforcement unless we are required to do so by court order, subpoena, search warrant or other requests that we determine are legally valid. https://www.23andme.com/privacy/ fridec2 发表于 2023-11-18 14:03
We will not share your genetic data with employers, insurance companies, public databases or 3rd party marketers without your explicit consent. We will not release any individual-level personal information to law enforcement unless we are required to do so by court order, subpoena, search warrant or other requests that we determine are legally valid. https://www.23andme.com/privacy/ fridec2 发表于 2023-11-18 14:03
为啥要测dna，家里有皇位要继承吗
不是，可以在上面找亲戚。也可以测一些潜在疾病的基因。
测这个要实名吗？
中国也有DNA数据库吧。
哈哈， 不是，就是觉得挺有意思。想知道自己DNA profile.
哦，原来如此，那就不好奇了。 多谢。
古哥也是，你能不上网吗？
We will not release any individual-level personal information to law enforcement unless we are required to do so by court order, subpoena, search warrant or other requests that we determine are legally valid.
https://www.23andme.com/privacy/
多谢解答。看着描述也是这么说的，觉得挺好奇的。不过有些回复的concern也非常有道理。我就收了我的好奇心吧。
忘了上次他们数据库被hack了？ https://www.dailymail.co.uk/news/article-12646383/23andMe-breach-hacker-royal-family.html 连英国皇室的基因都被泄露了 据说这个基因数据可以用来做定向武器的哦
Sema4已经倒闭了。
court order太容易了
真的啊！
有不少疾病预警的。糖尿病几率啥的的都很准。样本大于五。
疾病预警难道不是自己家族病史最准确？靠基因有点杀鸡用牛刀
这些公司都被医院控制 可以改数据的
我家娃被基因公司动过手脚。 。。
他们的亚洲人基因库很小，测不出个啥如果你的目的是看lineage的话。
要是测民族的话，国内的数据库更准，你可以把23andme的数据上传到国内的微基因app上。
国内我试过，只说我是99.5%的北方汉族，超级无聊。好歹23andme还说我有过欧洲中亚的祖先什么的。
还要填问卷？那不测了
预测乳房癌之类的吗？
有BRCA1/2。 大概一共有60种遗传疾病的可能性分析。 另外还有45种身体特征，运动能力，睡眠质量，饮食偏好，甚至唱歌五音不全的分析。 如果多花钱买23andme+还能得到更多的分析报告，我就是用的Amazon打折时买的基本款。 下面是我的报告项目，结果隐掉了。 Health Predisposition Age-Related Macular DegenerationVariant Alpha-1 Antitrypsin DeficiencyVariants BRCA1/BRCA2 (Selected Variants)Variants Celiac DiseaseVariants Chronic Kidney Disease (APOL1-Related)Variants Familial HypercholesterolemiaVariants G6PD DeficiencyVariants Hereditary Amyloidosis (TTR-Related)Variants Hereditary Hemochromatosis (HFE‑Related)Variants Hereditary ThrombophiliaVariants Late-Onset Alzheimer''''s DiseaseVariant MUTYH-Associated PolyposisVariants Parkinson''''s DiseaseVariants Type 2 DiabetesTypical Carrier Status ARSACSVariant Agenesis of the Corpus Callosum with Peripheral NeuropathyVariant Autosomal Recessive Polycystic Kidney DiseaseVariant Beta Thalassemia and Related HemoglobinopathiesVariant Bloom SyndromeVariant Canavan DiseaseVariant Congenital Disorder of Glycosylation Type 1a (PMM2-CDG)Variant Cystic FibrosisVariant D-Bifunctional Protein DeficiencyVariant Dihydrolipoamide Dehydrogenase DeficiencyVariant Familial DysautonomiaVariant Familial Hyperinsulinism (ABCC8-Related)Variant Familial Mediterranean FeverVariant Fanconi Anemia Group CVariant GRACILE SyndromeVariant Gaucher Disease Type 1Variant Glycogen Storage Disease Type IaVariant Glycogen Storage Disease Type IbVariant Hereditary Fructose IntoleranceVariant Leigh Syndrome, French Canadian TypeVariant Limb-Girdle Muscular Dystrophy Type 2DVariant Limb-Girdle Muscular Dystrophy Type 2EVariant Limb-Girdle Muscular Dystrophy Type 2IVariant MCAD DeficiencyVariant Maple Syrup Urine Disease Type 1BVariant Mucolipidosis Type IVVariant Neuronal Ceroid Lipofuscinosis (CLN5-Related)Variant Neuronal Ceroid Lipofuscinosis (PPT1-Related)Variant Niemann-Pick Disease Type AVariant Nijmegen Breakage SyndromeVariant Nonsyndromic Hearing Loss and Deafness, DFNB1 (GJB2-Related)Variant Pendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related)Variant Phenylketonuria and Related DisordersVariant Pompe DiseaseVariant Primary Hyperoxaluria Type 2Variant Pyruvate Kinase DeficiencyVariant Rhizomelic Chondrodysplasia Punctata Type 1Variant Salla DiseaseVariant Severe Junctional Epidermolysis Bullosa (LAMB3-Related)Variant Sickle Cell AnemiaVariant Sjögren-Larsson SyndromeVariant Tay-Sachs DiseaseVariant Tyrosinemia Type IVariant Usher Syndrome Type 1FVariant Usher Syndrome Type 3AVariant Zellweger Spectrum Disorder (PEX1-Related)Variant Wellness Alcohol Flush Reaction Caffeine Consumption Deep SleepLess Genetic Weight Lactose Intolerance Muscle Composition Common in elite power athletes Saturated Fat and Weight Sleep Movement Traits Ability to Match Musical Pitch Asparagus Odor Detection Back Hair Bald Spot Bitter Taste BunionsLess Cheek Dimples Cilantro Taste Cleft Chin Dandruff Earlobe Type Early Hair Earwax Type Eye Color Fear of Heights Fear of Public Speaking Finger Length Ratio Flat Feet Freckles Hair Photobleaching Hair Texture Hair Thickness Ice Cream Flavor Preference Light or Dark Hair Misophonia Mosquito Bite Frequency Motion Sickness Newborn Hair Photic Sneeze Reflex Red Hair Skin Pigmentation Stretch Marks Sweet vs. Salty Toe Length Ratio Unibrow Wake-Up Time Widow''''s Peak
谢谢啊！brca1/2就是
哦，对对。 我记得当时仔细看报告的时候有的，刚才匆匆忙忙贴过来的时候没有scan到cancer就以为没有了，还赶快编辑了帖子"修正"没有
又没皇位要继承，普通老百姓拿这点隐私做绊脚石头干嘛
没看明白，为啥更新基因库是无耻的行为？难道他们得到了更多的数据，看到了更多的汉族基因，不就是应该更新自己的模型么？要是不更新，才无耻呢。
汉族本来就是个融合民族，汉族自身的南北差异连肉眼都能看出来。所以他们数据多了，就可以更好的预测了。那个数据科学预测，扩充训练集训练模型提高精度，是首要的吧。最后肯定是见得越多越准确。更何况，民族这个东西，还有很多文化上的，比如从外族收养来的，几代以后，也就被加入到自己的民族序列里了。
比如刚开始可能觉得基因A是蒙古族更多，所以标记成蒙古族，但是数据多了之后，发现基因A和基因B共同存在的话，汉族会更多，而基因B不存在，那还是蒙古族更多，这个精度就会提高，结果也更准确。
最简单的例子给我家孩子做的公司， 不是做出来了， 而是把原始数据给我们了。
几个月后公司就被关闭了！ 而这个公司一开始还说采访我， 因为我是第一个拿到他们公司原始数据的。 是他们愿意让我们下载到手的。 有了原始数据就可以判断出美国一大堆医院的实验室作假 baylor, cchmc, genedx, 等等。。。
所以关键东西隐瞒， 其他不是太关键的随便胡说 也就是很显然了。
可以先说你的胆固醇太高了 十年后你还活着 可能再卖个verison 说你就应该比别人高。
这种事情跟利益挂钩， 跟医院挂钩， 绝对没有啥用处， 除了骗人。