Genetic Predisposition to DiseaseDisease SusceptibilityGenetic LinkagePolymorphism, Single NucleotideGenotypeChromosome MappingAllelesHaplotypesLod ScoreLinkage DisequilibriumGenome-Wide Association StudyGene FrequencyCase-Control StudiesMicrobial Sensitivity TestsPolymorphism, GeneticGenetic MarkersBRCA1 ProteinPhenotypeBRCA2 ProteinPedigreeSmall Ubiquitin-Related Modifier ProteinsMutationGenes, BRCA1Genetic TestingChromosomes, Human, Pair 6Microsatellite RepeatsGenome, HumanGenetic VariationGenetic Association StudiesGenetic LociFamily HealthAnti-Bacterial AgentsChromosomes, Human, Pair 1Germ-Line MutationHeterozygoteSchizophreniaAge of OnsetMolecular Sequence DataModels, GeneticGenetic HeterogeneityEpistasis, GeneticBreast NeoplasmsGenes, RetinoblastomaGenes, BRCA2Quantitative Trait LociChromosomes, Human, Pair 2Crosses, GeneticAsian Continental Ancestry GroupSUMO-1 ProteinPenetrancePolymerase Chain ReactionDiabetes Mellitus, Type 1Mice, CongenicRisk FactorsChromosomes, Human, Pair 13Transcription FactorsNuclear FamilyChromosomes, Human, Pair 5Neoplastic Syndromes, HereditaryCarrier ProteinsFamilyDNA Mutational AnalysisDNA-Binding ProteinsRetinoblastoma ProteinEuropean Continental Ancestry GroupMice, Inbred C57BLLupus Erythematosus, SystemicChromosomes, Human, Pair 20Endosomal Sorting Complexes Required for TransportChromosomes, Human, Pair 10SumoylationDisease Models, AnimalHomozygoteBase SequenceDrug Resistance, BacterialGenes, DominantNod2 Signaling Adaptor ProteinDrug Resistance, MicrobialExonsNuclear ProteinsChromosomes, Human, Pair 17Sequence Analysis, DNAMultifactorial InheritanceProtein Tyrosine Phosphatase, Non-Receptor Type 22PsoriasisRetinoblastomaAmino Acid SequenceMutation, MissenseNeoplasm ProteinsOvarian NeoplasmsNerve Tissue ProteinsAnimals, CongenicSpecies SpecificityHeterozygote DetectionAutistic DisorderHLA-DRB1 ChainsDiabetes Mellitus, Type 2Cell LineMice, KnockoutChromosomes, Human, Pair 3