Description

family-based linkage maps/ recombination
genome wide association studies/ linkage disequilibrium
way to find the correlation and regression value of traits
DNA sequence variation occurring with a single nucleotide
disease caused by a single mutated gene
factors that one is testing upon
factors left alone and not tested upon
non-persistence allele
how likely someone is to have the disease if they have the risk allele
moods swings ragging from high to low manic episodes
chronic inflammatory disorder affective the joints
homozygous trait
heterozygous trait
heterozygous individuals have intermediate phenotype
have either one or two copies of the associated genetic variant
have two copies of the associated genetic variant/heterozygous individuals are carriers
variation of two types inflectional and derivational for genes
variation defined as the variance of the breeding values among individuals
value derived from the mass and height of a person
specific physical location of a gene or other DNA sequence on a chromosome
traits that correlate with variation of a phenotype of a population
disease caused by the interaction of multiple genes and environmental factors
region sequence of DNA to which proteins bind that initiate transcription
region of DNA or RNA that codes for protein
sections of the genome are repeated and the number of repeats in the genome varies between individuals

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Mendelian Genetics

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WS 6

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Genetics

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Heredity/Meiosis

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Vocab

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Genetics Review

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