Point MutationMutation, MissenseMutationGenetic Predisposition to DiseaseFrameshift MutationGenotypePolymorphism, Single NucleotideGerm-Line MutationAllelesPedigreeGenetic TestingHeterozygoteGenetic CounselingGenome-Wide Association StudyRisk FactorsMutation RateGene FrequencyExonsBase SequencePolymerase Chain ReactionCase-Control StudiesAmino Acid SubstitutionPhenotypePolymorphism, GeneticDNA Mutational AnalysisHomozygoteMolecular Sequence DataApolipoprotein E4Family HealthGenetic VariationGenetic LociGenetic Association StudiesPolymorphism, Single-Stranded ConformationalSequence Analysis, DNAMutagenesis, Site-DirectedHeterozygote DetectionModels, GeneticGenes, RecessiveAmino Acid SequenceCodon, NonsenseMutagenesisAge of OnsetGenetic LinkageChromosome MappingAsian Continental Ancestry GroupGene-Environment InteractionGenes, DominantGenetic MarkersGenes, BRCA1Diseases in TwinsDNA PrimersFactor VSequence DeletionLinkage DisequilibriumHaplotypesRiskGenes, BRCA2Protein Structure, TertiaryCohort StudiesDNA-Binding ProteinsGene DeletionEscherichia coliSuppression, GeneticFamilyAlzheimer DiseaseDNAModels, MolecularMembrane ProteinsEuropean Continental Ancestry GroupTranscription FactorsSchizophreniaCodonRisk AssessmentHLA-DRB1 ChainsEndophenotypesCell LinePenetranceBinding SitesGenetic Diseases, InbornSequence Homology, Amino AcidGenetic Complementation TestGenome, HumanApolipoproteins EFounder EffectPromoter Regions, GeneticGenes, p53SyndromeCloning, MolecularProtein BindingSequence AlignmentMutant ProteinsHLA-DQ AntigensMultifactorial InheritanceIntronsTwins, MonozygoticSaccharomyces cerevisiaeConsanguinityCarrier ProteinsBacterial ProteinsPlasmids