Polymorphism, Single NucleotideGenotypeHaplotypesLinkage DisequilibriumGenome-Wide Association StudyGenetic Predisposition to DiseaseGene FrequencyGenetic Association StudiesAllelesCase-Control StudiesGenetic VariationGenome, HumanGenetic LociAsian Continental Ancestry GroupSequence Analysis, DNAEuropean Continental Ancestry GroupGenetic MarkersChromosome MappingGenotyping TechniquesPhenotypeQuantitative Trait LociModels, GeneticHapMap ProjectGenetics, PopulationDatabases, GeneticGenetic LinkageRisk FactorsPolymorphism, GeneticEpistasis, GeneticSoftwareChinaGenomicsINDEL MutationCohort StudiesAlgorithmsComputational BiologyPharmacogeneticsAfrican AmericansPolymerase Chain ReactionBase SequenceExpressed Sequence TagsMicrosatellite RepeatsDNA Mutational AnalysisExonsGenomeDatabases, Nucleic AcidHomozygoteOligonucleotide Array Sequence AnalysisOdds RatioIntronsGene-Environment InteractionChromosomes, Human, Pair 6HeterozygoteDiabetes Mellitus, Type 2RiskAfrican Continental Ancestry GroupHigh-Throughput Nucleotide SequencingReproducibility of ResultsMolecular Sequence DataDiseaseChromosomes, Human, Pair 9Principal Component AnalysisGenetic TestingMultifactorial InheritancePromoter Regions, GeneticEthnic GroupsPopulation GroupsChromosomes, Human, Pair 103' Untranslated RegionsSelection, GeneticComputer SimulationMolecular Sequence AnnotationAge of OnsetQuantitative Trait, HeritableInheritance PatternsPedigreeGenome, PlantLogistic ModelsDNABreedingChromosomes, HumanChromosomes, Human, Pair 1Polymorphism, Restriction Fragment LengthMutationChromosomes, Human, Pair 5Chromosomes, Human, Pair 2JapanModels, StatisticalPhylogenyDNA Copy Number VariationsExfoliation SyndromeBayes TheoremDNA PrimersTranscription Factor 7-Like 2 ProteinChromosomes, Human, Pair 8User-Computer InterfaceContig MappingFamilyInternetSchizophrenia