Linkage DisequilibriumPolymorphism, Single NucleotideHaplotypesPolymorphism, GeneticGenetic LinkageAllelesGene FrequencyGenetic MarkersGenotypeGenetic Predisposition to DiseaseGenetics, PopulationChromosome MappingGenetic VariationModels, GeneticMicrosatellite RepeatsQuantitative Trait LociGenome-Wide Association StudyCase-Control StudiesPedigreeGenome, HumanSelection, GeneticEuropean Continental Ancestry GroupRecombination, GeneticAsian Continental Ancestry GroupGenetic LociGenetic Association StudiesPhenotypeFounder EffectSequence Analysis, DNAHeterozygotePolymerase Chain ReactionQuantitative Trait, HeritableLod ScoreMolecular Sequence DataPolymorphism, Restriction Fragment LengthBase SequenceComputer SimulationGenetic Diseases, InbornHomozygoteLikelihood FunctionsChromosomes, Human, Pair 6Nuclear FamilyEpistasis, GeneticGenotyping TechniquesExonsModels, StatisticalChromosomes, Human, Pair 1HapMap ProjectIntronsGenetic HeterogeneityAmplified Fragment Length Polymorphism AnalysisPolymorphism, Single-Stranded ConformationalHLA-DRB1 ChainsAlgorithmsChromosomes, Human, Pair 12MutationBreedingSample SizeRisk FactorsEvolution, MolecularPhylogenyChinaAfrican Continental Ancestry GroupSoftwareGenetic TestingPhysical Chromosome MappingHLA-DQ beta-ChainsChromosomes, Human, Pair 19GenomePromoter Regions, GeneticDNAPopulationDNA PrimersGenome, PlantMinisatellite RepeatsDNA Mutational AnalysisChromosome InversionHLA AntigensChromosomes, Human, Pair 5JapanHeterozygote DetectionEthnic GroupsEuropeHLA-DQ AntigensGenes, DominantChromosomes, HumanChromosomes, Human, Pair 2Cohort StudiesGenes, RecessiveChromosomes, Human, Pair 16AfricaFamily HealthTandem Repeat SequencesINDEL MutationAge of OnsetMultigene FamilyGenomicsCrosses, GeneticJewsChromosomes, Human, X