Polymorphism, Single NucleotideGenetic VariationGenome-Wide Association StudyGenetic Predisposition to DiseaseGenotypeGene FrequencyAllelesHaplotypesCase-Control StudiesGenetic Association StudiesLinkage DisequilibriumMultifactorial InheritancePolymorphism, GeneticGenetic LociEuropean Continental Ancestry GroupAsian Continental Ancestry GroupPhenotypeGenome, HumanRisk FactorsExomeMutationMolecular Sequence DataSequence Analysis, DNADiabetes Mellitus, Type 2HomozygoteTranscription Factor 7-Like 2 ProteinCohort StudiesMeta-Analysis as TopicChromosomes, Human, Pair 9ExonsModels, GeneticGenetic MarkersChromosomes, Human, Pair 6Base SequenceHeterozygoteReceptor, Melanocortin, Type 4Quantitative Trait LociMutation, MissenseHapMap ProjectAmino Acid SubstitutionAmino Acid SequenceChromosome MappingOdds RatioReceptor, Melatonin, MT2Chromosomes, Human, Pair 8ChinaPolymerase Chain ReactionGenetics, PopulationAlternative SplicingGenetic LinkageGenetic TestingKCNQ1 Potassium ChannelPharmacogeneticsAge of OnsetHepatocyte Nuclear Factor 1-betaRiskDNA Mutational AnalysisIntronsChromosomes, Human, Pair 12TCF Transcription FactorsReceptor, EphA1Ethnic GroupsMembrane ProteinsObesityUromodulinPedigreeChromosomes, Human, Pair 1NAV1.5 Voltage-Gated Sodium ChannelBreast NeoplasmsEpistasis, GeneticProteinsFar EastAfrican AmericansDNA Copy Number VariationsBody Mass IndexItalySchizophreniaFinlandCyclin-Dependent Kinase Inhibitor p15Quantitative Trait, HeritableHepatocyte Nuclear Factor 1-alphaChild Development Disorders, PervasiveEuropePromoter Regions, GeneticSiblingsGene-Environment InteractionHigh-Throughput Nucleotide SequencingGenetic HeterogeneityAdaptor Proteins, Signal TransducingDNA-Binding ProteinsTranscription FactorsFamily HealthDNA PrimersChromosomes, Human, Pair 4African Continental Ancestry Group3' Untranslated RegionsRNA, MessengerGenes, BRCA2Long QT SyndromeCell Line