Andrei DNA is a youtuber that makes very rich analysis of humans genome. He has built plenty of tools about genome and phenotype prediction and the latest one analyzes your genome on the following subjects: Mental Health, Lactose Persistence, OXTR or the empathy gene, Diabetes, Hemochromatosis, Alzheimers, Myopia, Albinism and some more.
You can find his most spectacular channel here: https://www.youtube.com/@-andreiDNA
His latest tool: https://andreikharchenko1.github.io/Trait-Predictor/
Here are some results of my analysis based on this tool:
Mental health:
Albruic has AG in COMT's Val/Met variation, meaning Val/Met genotype, intermediate speed of dopamine reuptake, and intermediate dopamine levels.
This individual has GG, which means no derived No-Go Learner variants in DRD2's Pro319Pro variation, which means a higher number of D2 receptor sites in the brain, and a higher likelihood of schizophrenia
This individual has GG genotype in Taq1 variation of DRD2, which is the typical genotype for most humans leading to a slightly higher number of D2 dopamine receptors, and to a slightly lower risk of ADHD and Alcoholism.
This individual has CC genotype in rs5326 of DRD1, which is the typical genotype for most humans and leads to a slightly lower risk of various mental health conditions.
This individual has AG genotype in rs686 of Dopamine Receptor D1 gene, which leads to a slightly higher likelyhood of Autism and tobacco addiction.
This individual has TC, or heterozygous genotype in rs4532 of DRD1, which is implicated in slightly lower odds of Autism and tobacco addiction.
This individual has AG genotype in rs265981 of DRD1, which is implicated in lower odds of various mental illnesses in Europeans.
This individual has TT genotype in rs2129785, a typical genotype for most humans. The implications of this genotype is that this individual does not have long form 5-HTTLPR and does not have a decrease in the risk of depression.
Lactose persistance:
This individual has GG in MCM6's rs4988235 variation, which means this individual does not carry the European lactose persistence mutation.
Empathy gene:
This individual has GG in OXTR's rs53576 variation, which means this individual has 2 variants for higher levels of empathy at this variation.
Diabetes:
This individual has CC genotype in rs9273363, which leads to a 7 fold decrease in the risk of type 1 diabetes.
This individual has CG in rs7754840, which means this individual has one variant for higher odds of type 2 diabetes.
This individual has CC genotype in rs7903146, a genotype associated with lower risk of type 2 diabetes.
This individual has GG genotype in rs4402960, leading to slight decrease in the risk of Type 2 Diabetes.
Myopia:
This individual has AA in rs12193446, which is the typical genotype and leads to slightly increased risk of myopia, or nearsightedness.
This individual has AA genotype in rs7744813, which leads to a decrease in the risk of myopia.
This individual has Genotype for rs524952 Not Determined
This individual has CC genotype in rs4803455, two alleles for increased Myopia risk.
Miscellaneous:
This individual has CT genotype in rs10784502, slightly increased cranial size and 1% higher IQ.
This individual has CT genotype in rs28379706, slightly higher IQ.
This individual has AG in rs324640, 4 points higher IQ than individuals with 'AA' genotype.
This individual has CT genotype in rs1815739, Mix of muscle types. Likely more sprinter than endurance athlete.
This individual has TT genotype, No 'fat gene' variants in FTO's rs9939609.
Drug response:
This individual has TT genotype in AKT1's rs2494732, lower odds of Cannabis induced psychosis.
This individual has AA genotype in rs2241802, lower odds of methamphatamine induced psychosis.
This individual has CC in rs135745, higher susceptibility to methamphetamine induced psychosis.
Albinism and Atypical traits:
This individual has AA in TYR's rs28940881 variation, which means this individual does not have any Tyrosinase-negative oculocutaneous albinism mutations.
This individual has TT genotype in rs61754381, which means not a carrier for 1B Tyrosinase-negative oculocutaneous albinism.
This individual has CC genotype in rs987525, which leads to decreased risk of cleft lip and palate.
You can find his most spectacular channel here: https://www.youtube.com/@-andreiDNA
His latest tool: https://andreikharchenko1.github.io/Trait-Predictor/
Here are some results of my analysis based on this tool:
Mental health:
Albruic has AG in COMT's Val/Met variation, meaning Val/Met genotype, intermediate speed of dopamine reuptake, and intermediate dopamine levels.
This individual has GG, which means no derived No-Go Learner variants in DRD2's Pro319Pro variation, which means a higher number of D2 receptor sites in the brain, and a higher likelihood of schizophrenia
This individual has GG genotype in Taq1 variation of DRD2, which is the typical genotype for most humans leading to a slightly higher number of D2 dopamine receptors, and to a slightly lower risk of ADHD and Alcoholism.
This individual has CC genotype in rs5326 of DRD1, which is the typical genotype for most humans and leads to a slightly lower risk of various mental health conditions.
This individual has AG genotype in rs686 of Dopamine Receptor D1 gene, which leads to a slightly higher likelyhood of Autism and tobacco addiction.
This individual has TC, or heterozygous genotype in rs4532 of DRD1, which is implicated in slightly lower odds of Autism and tobacco addiction.
This individual has AG genotype in rs265981 of DRD1, which is implicated in lower odds of various mental illnesses in Europeans.
This individual has TT genotype in rs2129785, a typical genotype for most humans. The implications of this genotype is that this individual does not have long form 5-HTTLPR and does not have a decrease in the risk of depression.
Lactose persistance:
This individual has GG in MCM6's rs4988235 variation, which means this individual does not carry the European lactose persistence mutation.
Empathy gene:
This individual has GG in OXTR's rs53576 variation, which means this individual has 2 variants for higher levels of empathy at this variation.
Diabetes:
This individual has CC genotype in rs9273363, which leads to a 7 fold decrease in the risk of type 1 diabetes.
This individual has CG in rs7754840, which means this individual has one variant for higher odds of type 2 diabetes.
This individual has CC genotype in rs7903146, a genotype associated with lower risk of type 2 diabetes.
This individual has GG genotype in rs4402960, leading to slight decrease in the risk of Type 2 Diabetes.
Myopia:
This individual has AA in rs12193446, which is the typical genotype and leads to slightly increased risk of myopia, or nearsightedness.
This individual has AA genotype in rs7744813, which leads to a decrease in the risk of myopia.
This individual has Genotype for rs524952 Not Determined
This individual has CC genotype in rs4803455, two alleles for increased Myopia risk.
Miscellaneous:
This individual has CT genotype in rs10784502, slightly increased cranial size and 1% higher IQ.
This individual has CT genotype in rs28379706, slightly higher IQ.
This individual has AG in rs324640, 4 points higher IQ than individuals with 'AA' genotype.
This individual has CT genotype in rs1815739, Mix of muscle types. Likely more sprinter than endurance athlete.
This individual has TT genotype, No 'fat gene' variants in FTO's rs9939609.
Drug response:
This individual has TT genotype in AKT1's rs2494732, lower odds of Cannabis induced psychosis.
This individual has AA genotype in rs2241802, lower odds of methamphatamine induced psychosis.
This individual has CC in rs135745, higher susceptibility to methamphetamine induced psychosis.
Albinism and Atypical traits:
This individual has AA in TYR's rs28940881 variation, which means this individual does not have any Tyrosinase-negative oculocutaneous albinism mutations.
This individual has TT genotype in rs61754381, which means not a carrier for 1B Tyrosinase-negative oculocutaneous albinism.
This individual has CC genotype in rs987525, which leads to decreased risk of cleft lip and palate.