Genetic variants genes brca2. Medical search. Frequent questions

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Anatomy8

Tumor Cells, Cultured Cell Line Cell Line, Tumor Chromosomes, Human, Pair 9 Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 6 Chromosomes, Human, Pair 15 Chromosomes, Human, Pair 8

Organisms1

Escherichia coli

Diseases7

Genetic Predisposition to Disease Breast Neoplasms Ovarian Neoplasms Diabetes Mellitus, Type 2 Breast Neoplasms, Male Neoplastic Syndromes, Hereditary Prostatic Neoplasms

Chemicals and Drugs21

BRCA1 Protein BRCA2 Protein Rad51 Recombinase Neoplasm Proteins Transcription Factors Genetic Markers Transcription Factor 7-Like 2 Protein Protein Isoforms DNA-Binding Proteins RNA, Messenger DNA Primers Aryl Hydrocarbon Hydroxylases Tumor Suppressor Proteins Nuclear Proteins DNA Carrier Proteins DNA, Neoplasm Ubiquitin-Protein Ligases Membrane Proteins Methylenetetrahydrofolate Reductase (NADPH2)Vitamin K Epoxide Reductases

Analytical, Diagnostic and Therapeutic Techniques and Equipment25

Genome-Wide Association Study Genetic Testing Case-Control Studies Genetic Association Studies Risk Factors Sequence Analysis, DNA DNA Mutational Analysis Pedigree Cohort Studies Polymerase Chain Reaction Models, Genetic Risk Genotyping Techniques Odds Ratio Mendelian Randomization Analysis Chromosome Mapping Amino Acid Substitution Risk Assessment Meta-Analysis as Topic Logistic Models High-Throughput Nucleotide Sequencing Reverse Transcriptase Polymerase Chain Reaction Models, Statistical Heterozygote Detection Salpingectomy

Phenomena and Processes61

Genes, BRCA1 Genes, BRCA2 Genetic Variation Base Sequence Genetic Predisposition to Disease Polymorphism, Single Nucleotide Amino Acid Sequence Germ-Line Mutation Genotype Heterozygote Mutation DNA Repair Gene Frequency Alleles Haplotypes Polymorphism, Genetic DNA Damage Phenotype Linkage Disequilibrium Genetic Loci Genome, Human Exons Homozygote Alternative Splicing Genetic Markers Mutation, Missense Risk Quantitative Trait Loci Gene-Environment Interaction Exome Odds Ratio Founder Effect Epistasis, Genetic Genetic Linkage Promoter Regions, Genetic Amino Acid Substitution Multifactorial Inheritance Penetrance Chromosomes, Human, Pair 9 Inheritance Patterns Introns Protein Binding Sequence Deletion Protein Structure, Tertiary Point Mutation Polymorphism, Restriction Fragment Length Genetic Pleiotropy Gene Expression Regulation, Neoplastic Phylogeny Chromosomes, Human, Pair 10 DNA Copy Number Variations Polymorphism, Single-Stranded Conformational Genetic Heterogeneity Gene Expression Regulation Frameshift Mutation Chromosomes, Human, Pair 6 Algorithms Binding Sites Chromosomes, Human, Pair 15 Gene Deletion Chromosomes, Human, Pair 8

Disciplines and Occupations5

Pharmacogenetics HapMap Project Genetics, Population Genetic Counseling Genomics

Information Science6

Molecular Sequence Data Base Sequence Amino Acid Sequence Phylogeny Algorithms Databases, Genetic

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European Continental Ancestry Group Asian Continental Ancestry Group Jews African Continental Ancestry Group African Americans Ethnic Groups Population Groups

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Genome-Wide Association Study Genetic Testing Case-Control Studies Risk Factors Cohort Studies Risk Odds Ratio Family Health Genetic Counseling Risk Assessment Meta-Analysis as Topic Logistic Models Models, Statistical Ethnic Groups Population Groups

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Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Phenomena and Processes Disciplines and Occupations Information Science Named Groups Health Care Geographicals

BRCA1 Protein Genes, BRCA1 BRCA2 Protein Genes, BRCA2 Genetic Variation Molecular Sequence Data Base Sequence Genetic Predisposition to Disease Polymorphism, Single Nucleotide Breast Neoplasms Amino Acid Sequence Germ-Line Mutation Escherichia coli Ovarian Neoplasms Genotype Heterozygote Mutation Genome-Wide Association Study Genetic Testing Rad51 Recombinase Neoplasm Proteins DNA Repair Gene Frequency Case-Control Studies Alleles Haplotypes Genetic Association Studies Polymorphism, Genetic DNA Damage Transcription Factors Phenotype Linkage Disequilibrium European Continental Ancestry Group Risk Factors Asian Continental Ancestry Group Genetic Loci Pharmacogenetics Tumor Cells, Cultured Jews Sequence Analysis, DNA DNA Mutational Analysis Genome, Human Exons Pedigree Cohort Studies Polymerase Chain Reaction Models, Genetic Homozygote Alternative Splicing Genetic Markers Mutation, Missense China Risk Genotyping Techniques Quantitative Trait Loci Gene-Environment Interaction Exome Odds Ratio Founder Effect HapMap Project Mendelian Randomization Analysis Epistasis, Genetic Genetic Linkage Promoter Regions, Genetic Chromosome Mapping Amino Acid Substitution Family Health Transcription Factor 7-Like 2 Protein Diabetes Mellitus, Type 2 Breast Neoplasms, Male Cell Line African Continental Ancestry Group Protein Isoforms Multifactorial Inheritance DNA-Binding Proteins Neoplastic Syndromes, Hereditary Penetrance African Americans RNA, Messenger Genetics, Population DNA Primers Genetic Counseling Risk Assessment Aryl Hydrocarbon Hydroxylases Cell Line, Tumor Tumor Suppressor Proteins Nuclear Proteins Chromosomes, Human, Pair 9 Inheritance Patterns Meta-Analysis as Topic DNA Introns Logistic Models Protein Binding Sequence Deletion Protein Structure, Tertiary Carrier Proteins Point Mutation Prostatic Neoplasms High-Throughput Nucleotide Sequencing

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