Genes with rare variants. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy14

Ulnar Artery Chromosomes, Human, Pair 22 Chromosomes, Human, Pair 15 Chromosomes, Human Cell Line Cells, Cultured HEK293 Cells Cell Line, Tumor Tumor Cells, Cultured COS Cells Brain HeLa Cells CHO Cells Clone Cells

Organisms6

Escherichia coli HIV-1 Cricetinae Cercopithecus aethiops Cattle Trypanosoma brucei brucei

Diseases20

Genetic Predisposition to Disease Rare Diseases Disease Porokeratosis Genetic Diseases, Inborn Truncus Arteriosus, Persistent Cleft Lip Neurofibromatoses Cardiovascular Abnormalities Cleft Palate Cardiomyopathy, Dilated Diabetes Mellitus, Type 1 Breast Neoplasms Angina Pectoris, Variant Diabetes Mellitus, Type 2 Obesity Skin Neoplasms Colorectal Neoplasms Creutzfeldt-Jakob Syndrome Glucosephosphate Dehydrogenase Deficiency

Chemicals and Drugs48

Angiopoietins Monoacylglycerol Lipases Cardiac Myosins Untranslated Regions NAV1.5 Voltage-Gated Sodium Channel Genetic Markers DEAD-box RNA Helicases Protein Isoforms DNA Primers Carrier Proteins DNA Nerve Tissue Proteins Troponin C Membrane Proteins Adaptor Proteins, Signal Transducing Homeodomain Proteins Variant Surface Glycoproteins, Trypanosoma RNA, Messenger Hemoglobins, Abnormal Recombinant Proteins DNA, Complementary Mutant Proteins Bacterial Proteins DNA-Binding Proteins Histones DNA, Viral Antibodies, Monoclonal Transcription Factors Peptide Fragments Receptor, Melanocortin, Type 1 Prealbumin Epitopes Recombinant Fusion Proteins Isoenzymes Proteins Codon Aryl Hydrocarbon Hydroxylases RNA Splice Sites RNA, Viral alpha 1-Antitrypsin Nuclear Proteins Peptides Transcription Factor 7-Like 2 Protein DNA, Bacterial Glycoproteins 3' Untranslated Regions Neoplasm Proteins Antigens, CD44

Analytical, Diagnostic and Therapeutic Techniques and Equipment60

Genome-Wide Association Study Genetic Association Studies Sequence Analysis, DNA Models, Genetic High-Throughput Nucleotide Sequencing Genotyping Techniques Case-Control Studies Pedigree Sequence Analysis DNA Mutational Analysis Genetic Testing Models, Statistical Data Interpretation, Statistical Molecular Epidemiology Sample Size Chromosome Mapping Bayes Theorem Meta-Analysis as Topic Amino Acid Substitution Principal Component Analysis Polymerase Chain Reaction Cohort Studies Likelihood Functions Risk Factors Sequence Alignment Cluster Analysis Regression Analysis Monte Carlo Method Reproducibility of Results Genetic Techniques Risk Probability Fatal Outcome Logistic Models Oligonucleotide Array Sequence Analysis Sensitivity and Specificity Odds Ratio Immunohistochemistry Obesity Statistics as Topic Models, Molecular Linear Models Cloning, Molecular Research Design Mutagenesis, Site-Directed Tomography, X-Ray Computed Prognosis Reverse Transcriptase Polymerase Chain Reaction Transfection Magnetic Resonance Imaging Protein Engineering Directed Molecular Evolution Electrophoresis, Polyacrylamide Gel Blotting, Western Isoelectric Focusing Crystallography, X-Ray Enzyme Stability Electrophoresis, Starch Gel Gene Expression Profiling Circular Dichroism

Psychiatry and Psychology6

Child Development Disorders, Pervasive Autistic Disorder Family Bipolar Disorder Schizophrenia Creutzfeldt-Jakob Syndrome

Phenomena and Processes97

Genetic Variation Exome Polymorphism, Single Nucleotide Gene Frequency Genetic Predisposition to Disease Genotype Alleles Multifactorial Inheritance Phenotype Haplotypes Genomic Structural Variation Genome, Human Mutation Linkage Disequilibrium Mutation, Missense Exons Inheritance Patterns Polymorphism, Genetic Genetic Loci Base Sequence Algorithms DNA Copy Number Variations Heterozygote Genetic Linkage Quantitative Trait, Heritable INDEL Mutation Amino Acid Sequence Homozygote Mutation Rate Amino Acid Substitution Alternative Splicing Genetic Heterogeneity Untranslated Regions Chromosomes, Human, Pair 22 Quantitative Trait Loci Selection, Genetic Chromosomes, Human, Pair 15 Genetic Markers Point Mutation Germ-Line Mutation Evolution, Molecular Polymorphism, Single-Stranded Conformational Chromosomes, Human Genes Risk Probability Multigene Family Genome Sensitivity and Specificity Odds Ratio Open Reading Frames Obesity Protein Structure, Tertiary Phylogeny Protein Binding Sequence Homology, Amino Acid Antigenic Variation Binding Sites Kinetics Introns Protein Conformation Promoter Regions, Genetic Transfection RNA Splicing Sequence Deletion Polymorphism, Restriction Fragment Length Transcription, Genetic Structure-Activity Relationship Gene Expression Species Specificity Gene Expression Regulation Plasmids Sequence Homology, Nucleic Acid Protein Structure, Secondary Mutagenesis Virus Replication Substrate Specificity Virulence Conserved Sequence Drug Resistance, Viral Codon Protein Folding Gene Deletion Recombination, Genetic Gene Dosage RNA Splice Sites Enzyme Stability Signal Transduction Time Factors Genome, Viral Drug Resistance Organ Specificity Gene Library Hair Color Glycosylation 3' Untranslated Regions Frameshift Mutation

Disciplines and Occupations11

Human Genome Project HapMap Project Genetics, Population Molecular Epidemiology Genomics Computational Biology Pharmacogenetics Empirical Research Immunohistochemistry Statistics as Topic Research Design

Anthropology, Education, Sociology and Social Phenomena1

Information Science12

Human Genome Project Computer Simulation Molecular Sequence Data Base Sequence Algorithms Data Interpretation, Statistical Software Amino Acid Sequence Databases, Genetic Monte Carlo Method Fatal Outcome Phylogeny

Named Groups5

European Continental Ancestry Group Indians, South American Asian Continental Ancestry Group African Americans African Continental Ancestry Group

Health Care25

Genome-Wide Association Study Case-Control Studies Genetic Testing Models, Statistical Data Interpretation, Statistical Molecular Epidemiology Sample Size Bayes Theorem Meta-Analysis as Topic Cohort Studies Likelihood Functions Risk Factors Cluster Analysis Regression Analysis Monte Carlo Method Reproducibility of Results Risk Probability Fatal Outcome Age of Onset Logistic Models Sensitivity and Specificity Odds Ratio Statistics as Topic Linear Models

Geographicals2

Great Britain China

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

Genetic Variation Exome Genome-Wide Association Study Polymorphism, Single Nucleotide Genetic Association Studies Human Genome Project Gene Frequency Genetic Predisposition to Disease Sequence Analysis, DNA Models, Genetic Genotype HapMap Project High-Throughput Nucleotide Sequencing Alleles Genotyping Techniques Multifactorial Inheritance Phenotype Haplotypes Case-Control Studies Genomic Structural Variation Genome, Human Pedigree Mutation Angiopoietins Computer Simulation Genetics, Population Linkage Disequilibrium Mutation, Missense Exons Inheritance Patterns Sequence Analysis Rare Diseases Polymorphism, Genetic DNA Mutational Analysis Disease Molecular Sequence Data Genetic Loci Genetic Testing Base Sequence Porokeratosis Algorithms Models, Statistical DNA Copy Number Variations Heterozygote European Continental Ancestry Group Genetic Linkage Quantitative Trait, Heritable Monoacylglycerol Lipases Data Interpretation, Statistical Indians, South American Software Genetic Diseases, Inborn Molecular Epidemiology Sample Size INDEL Mutation Amino Acid Sequence Genomics Chromosome Mapping Computational Biology Ulnar Artery Bayes Theorem Meta-Analysis as Topic Cardiac Myosins Truncus Arteriosus, Persistent Homozygote Mutation Rate Amino Acid Substitution Cleft Lip Alternative Splicing Principal Component Analysis Polymerase Chain Reaction Genetic Heterogeneity Untranslated Regions Cohort Studies Child Development Disorders, Pervasive NAV1.5 Voltage-Gated Sodium Channel Autistic Disorder Neurofibromatoses Pharmacogenetics Chromosomes, Human, Pair 22 Quantitative Trait Loci Cardiovascular Abnormalities Selection, Genetic Databases, Genetic Chromosomes, Human, Pair 15 Family Cleft Palate Genetic Markers Cardiomyopathy, Dilated Empirical Research Likelihood Functions Risk Factors Point Mutation Asian Continental Ancestry Group Sequence Alignment Germ-Line Mutation DEAD-box RNA Helicases Evolution, Molecular Cluster Analysis African Americans

No FAQ available that match "genes with rare variants"