Genetic VariationPolymorphism, Single NucleotideGenetic Predisposition to DiseaseGenotypeGenome-Wide Association StudyGene FrequencyHaplotypesAllelesGenetic Association StudiesCase-Control StudiesPolymorphism, GeneticPhenotypeLinkage DisequilibriumEuropean Continental Ancestry GroupAsian Continental Ancestry GroupGenetic LociRisk FactorsMolecular Sequence DataPharmacogeneticsMutationSequence Analysis, DNAGenome, HumanBase SequenceHomozygoteChinaQuantitative Trait LociCohort StudiesAmino Acid SequenceGenotyping TechniquesGene-Environment InteractionModels, GeneticAlternative SplicingExomePolymerase Chain ReactionHeterozygoteGenetic MarkersExonsOdds RatioMendelian Randomization AnalysisRiskEpistasis, GeneticTranscription Factor 7-Like 2 ProteinAmino Acid SubstitutionDiabetes Mellitus, Type 2HapMap ProjectGenetic LinkageMutation, MissenseChromosome MappingGenetic TestingPedigreeAfrican Continental Ancestry GroupMultifactorial InheritanceDNA Mutational AnalysisProtein IsoformsAfrican AmericansAryl Hydrocarbon HydroxylasesGenetics, PopulationMeta-Analysis as TopicPromoter Regions, GeneticChromosomes, Human, Pair 9Inheritance PatternsCell LineBreast NeoplasmsDNA PrimersIntronsGenomicsLogistic ModelsPolymorphism, Restriction Fragment LengthPhylogenyPopulation GroupsChromosomes, Human, Pair 10Genetic PleiotropyRNA, MessengerHigh-Throughput Nucleotide SequencingDNADNA Copy Number VariationsVitamin K Epoxide ReductasesDiseaseEndophenotypesAge of OnsetEthnic GroupsBody Mass IndexRisk AssessmentMembrane ProteinsDatabases, GeneticChromosomes, Human, Pair 15Models, StatisticalMethylenetetrahydrofolate Reductase (NADPH2)Family HealthAlgorithmsReceptor, Melatonin, MT1Genetic HeterogeneityPoint MutationPenetranceLinear ModelsChromosomes, Human, Pair 5Chromosomes, Human, Pair 6GlucuronosyltransferaseObesityGene Expression Regulation