28. What are single nucleotide polymorphisms (SNPs)
(A) are two base-pair variations in the genomes of the human population
(B) are genetic markers used to study the genetic basis for disease
(C) are large nucleotide differences among individuals located in coding and non-coding sequences in the genome
(D) can not be the molecular basis for different alleles
(E) All of the listed responses are correct.

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