Identifies common genetic variants. Medical search. Frequent questions

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Anatomy16

Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 5 Cell Line Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 8 Chromosomes, Human, Pair 1 Chromosomes, Human, Pair 12 Brain Chromosomes, Human, Pair 20 Chromosomes, Human, Pair 11 HEK293 Cells Chromosomes, Human, Pair 3 Chromosomes, Human, Pair 7 Cell Line, Tumor

Organisms3

HIV-1 Neanderthals Anaplasma phagocytophilum

Diseases20

Genetic Predisposition to Disease Diabetes Mellitus, Type 2 Breast Neoplasms Obesity Disease Prostatic Neoplasms Macular Degeneration Angina Pectoris, Variant Colorectal Neoplasms Lung Neoplasms Coronary Artery Disease Genetic Diseases, Inborn Hypertension Disease Progression Disease Susceptibility Crohn Disease Alzheimer Disease Asthenozoospermia Asthma Long QT Syndrome

Chemicals and Drugs60

Genetic Markers Membrane Proteins Transcription Factor 7-Like 2 Protein Protein Isoforms Aryl Hydrocarbon Hydroxylases DNA Primers RNA, Messenger DNA Vitamin K Epoxide Reductases Methylenetetrahydrofolate Reductase (NADPH2)Receptor, Melatonin, MT1 Glucuronosyltransferase Catechol O-Methyltransferase Prealbumin Cyclin-Dependent Kinase Inhibitor p15 Carrier Proteins Proteins DNA-Binding Proteins Organic Cation Transport Proteins Arylamine N-Acetyltransferase Protein Tyrosine Phosphatase, Non-Receptor Type 22 Recombinant Proteins Orosomucoid Nerve Tissue Proteins Variant Surface Glycoproteins, Trypanosoma Glutathione Transferase Neoplasm Proteins 3' Untranslated Regions alpha 1-Antitrypsin Arylsulfotransferase Nod2 Signaling Adaptor Protein Transcription Factors Receptor, Melanocortin, Type 4 TCF Transcription Factors Serotonin Plasma Membrane Transport Proteins Lipase Antithrombin Proteins Adaptor Proteins, Signal Transducing Mutant Proteins ATP-Binding Cassette Transporters Cytochrome P-450 CYP2D6 Serum Albumin Complement Factor H Cholesterol, HDL Nuclear Proteins Biomarkers, Pharmacological Glutathione S-Transferase pi Organic Cation Transporter 1 Organic Anion Transporters NAV1.5 Voltage-Gated Sodium Channel Cytochrome P-450 CYP3A Codon Warfarin Isoenzymes Methylenetetrahydrofolate Dehydrogenase (NADP)Fatty Acid Desaturases Xeroderma Pigmentosum Group D Protein Vitamin D-Binding Protein Valine Hemoglobins, Abnormal

Analytical, Diagnostic and Therapeutic Techniques and Equipment46

Genome-Wide Association Study Case-Control Studies Genetic Association Studies Risk Factors Meta-Analysis as Topic Cohort Studies Odds Ratio Models, Genetic Risk Body Mass Index Linear Models Obesity Sequence Analysis, DNA Genotyping Techniques Polymerase Chain Reaction Mendelian Randomization Analysis Amino Acid Substitution Chromosome Mapping Genetic Testing Pedigree DNA Mutational Analysis Logistic Models High-Throughput Nucleotide Sequencing Risk Assessment Models, Statistical Models, Molecular Reverse Transcriptase Polymerase Chain Reaction Sequence Alignment Cloning, Molecular Reproducibility of Results Prospective Studies Molecular Epidemiology Individualized Medicine Oligonucleotide Array Sequence Analysis Regression Analysis Mutagenesis, Site-Directed Gene Expression Profiling Electrophoresis, Starch Gel Molecular Sequence Annotation Isoelectric Focusing Likelihood Functions Transfection Prognosis Chi-Square Distribution Blood Protein Electrophoresis ROC Curve

Psychiatry and Psychology6

Smoking Schizophrenia Siblings Genetics, Behavioral Alzheimer Disease Autistic Disorder

Phenomena and Processes86

Polymorphism, Single Nucleotide Genetic Variation Genetic Predisposition to Disease Genotype Alleles Gene Frequency Haplotypes Linkage Disequilibrium Genetic Loci Polymorphism, Genetic Phenotype Genome, Human Chromosomes, Human, Pair 9 Odds Ratio Chromosomes, Human, Pair 5 Quantitative Trait Loci Risk Body Mass Index Heterozygote Mutation Genetic Markers Obesity Base Sequence Homozygote Amino Acid Sequence Gene-Environment Interaction Alternative Splicing Exome Exons Epistasis, Genetic Amino Acid Substitution Genetic Linkage Mutation, Missense Multifactorial Inheritance Promoter Regions, Genetic Inheritance Patterns Introns Polymorphism, Restriction Fragment Length Phylogeny Chromosomes, Human, Pair 10 Genetic Pleiotropy DNA Copy Number Variations Endophenotypes Chromosomes, Human, Pair 15 Algorithms Genetic Heterogeneity Point Mutation Penetrance Chromosomes, Human, Pair 6 Gene Expression Regulation Chromosomes, Human, Pair 8 Quantitative Trait, Heritable Chromosomes, Human, Pair 1 Selection, Genetic Protein Binding Chromosomes, Human, Pair 12 Binding Sites Gene Expression Protein Structure, Tertiary Evolution, Molecular INDEL Mutation Species Specificity Kinetics Multigene Family 3' Untranslated Regions Sequence Homology, Amino Acid Chromosomes, Human, Pair 20 Signal Transduction Germ-Line Mutation Genes Transfection Chi-Square Distribution Sequence Deletion Disease Susceptibility RNA Splicing Chromosomes, Human, Pair 11 Protein Conformation Transcription, Genetic Gene Dosage Heredity Genome DNA Repair Chromosomes, Human, Pair 3 Codon Pregnancy Chromosomes, Human, Pair 7

Disciplines and Occupations10

Pharmacogenetics HapMap Project Genetics, Population Genomics Computational Biology Molecular Epidemiology Individualized Medicine Human Genome Project Genetics, Behavioral Genetics, Medical

Anthropology, Education, Sociology and Social Phenomena1

Information Science11

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Databases, Genetic Algorithms Software Computer Simulation Multifactor Dimensionality Reduction Human Genome Project Molecular Sequence Annotation

Named Groups10

European Continental Ancestry Group Asian Continental Ancestry Group African Americans African Continental Ancestry Group Population Groups Ethnic Groups Mexican Americans Hispanic Americans Siblings Infant, Newborn

Health Care25

Genome-Wide Association Study Case-Control Studies Risk Factors Meta-Analysis as Topic Cohort Studies Odds Ratio Risk Body Mass Index Linear Models Sex Factors Genetic Testing Logistic Models Population Groups Age of Onset Ethnic Groups Risk Assessment Models, Statistical Family Health Reproducibility of Results Prospective Studies Molecular Epidemiology Regression Analysis Likelihood Functions Chi-Square Distribution ROC Curve

Geographicals11

Finland China Germany Italy Japan Europe United States Spain Czech Republic Sweden Tibet

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Polymorphism, Single Nucleotide Genome-Wide Association Study Genetic Variation Genetic Predisposition to Disease Genotype Case-Control Studies Alleles Gene Frequency Haplotypes Linkage Disequilibrium Genetic Association Studies European Continental Ancestry Group Genetic Loci Polymorphism, Genetic Risk Factors Asian Continental Ancestry Group Meta-Analysis as Topic Phenotype Cohort Studies Genome, Human Chromosomes, Human, Pair 9 Diabetes Mellitus, Type 2 Odds Ratio Chromosomes, Human, Pair 5 Quantitative Trait Loci Models, Genetic Finland Risk Body Mass Index Heterozygote Mutation Genetic Markers Breast Neoplasms African Americans Linear Models Membrane Proteins Obesity Sex Factors Molecular Sequence Data Pharmacogenetics Sequence Analysis, DNA Base Sequence Homozygote China Amino Acid Sequence Genotyping Techniques Gene-Environment Interaction Alternative Splicing Exome Polymerase Chain Reaction Exons Mendelian Randomization Analysis Epistasis, Genetic Transcription Factor 7-Like 2 Protein Amino Acid Substitution HapMap Project Genetic Linkage Mutation, Missense Chromosome Mapping Genetic Testing Pedigree African Continental Ancestry Group Multifactorial Inheritance DNA Mutational Analysis Protein Isoforms Aryl Hydrocarbon Hydroxylases Genetics, Population Promoter Regions, Genetic Inheritance Patterns Cell Line DNA Primers Introns Genomics Logistic Models Polymorphism, Restriction Fragment Length Phylogeny Population Groups Chromosomes, Human, Pair 10 Genetic Pleiotropy RNA, Messenger High-Throughput Nucleotide Sequencing DNA DNA Copy Number Variations Vitamin K Epoxide Reductases Disease Endophenotypes Age of Onset Ethnic Groups Risk Assessment Databases, Genetic Chromosomes, Human, Pair 15 Models, Statistical Methylenetetrahydrofolate Reductase (NADPH2)Family Health Algorithms Receptor, Melatonin, MT1 Genetic Heterogeneity Point Mutation Penetrance Chromosomes, Human, Pair 6

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