Answer: The correct answer would be B
Answer:
SNPs have shown that only 0.1 % of DNA sequences are different in the human genome between different individuals, thereby all the inherited phenotypic variation observed in our species is associated with only 0.1 % of differences at the genome level
Explanation:
Haplotypes are block-like sequences of DNA that are inherited together due to low recombination rates. Moreover, single-nucleotide polymorphism (SNP) mapping is a very useful methodology used to map the site of SNP mutations (i.e., SNP variants). In this regard, it has been observed that there are approximately 10 million common SNPs in the human genome. These SNPs contribute to the wide range of phenotypic variation observed in human populations for different traits (e.g., eye color, hair, weight, height, etc). Moreover, researchers have determined that SNPs can be clustered into haplotypes, thereby haplotypes can be accurately sampled by as few as approx. 300,000 selected SNPs, which are sufficient to represent all of the genetic variation across different human genomes.
In chickens, the black wing allele is co-dominant with the white wing allele. Black and white birds are homozygous for the black (B) allele or the white (W) allele.
In genetics the terms, codominance refers to the pattern of inheritance in which the two versions (alleles) of the same gene are being expressed separately to produce the different traits in the individual. In perfect dominance, only the one allele of the genotype is also present in the phenotype. In codominant cases, both the alleles of the genotype are present in the phenotype. In the case of the imperfect dominance, the phenotype shows the mixture of genotypic alleles. In the genetics terms, codominance refers to the pattern of inheritance in which the two versions (alleles) of the same gene are expressed and separately to produce the different traits in the individual.
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