Answer:
C. considerable genetic polymorphism.
Explanation:
Single or simple nucleotide polymorphisms (from English Single Nucleotide Polymorphisms, SNPs), (pronounced as snips). They are the simplest and most common form of genetic polymorphism since they consist of changing a single nucleotide in the context of a genetic sequence. They are considered to determine most of the genetic variability among individuals, causing many of the phenotypic (observable) differences in them.
A SNP is a variation in the DNA sequence that affects a single nitrogenous base of a genome sequence: adenine (A), thymine (T), cytosine (C) or guanine (G). Some authors consider that changes of a few nucleotides, as well as small insertions and deletions (indels) can be considered as SNPs, if one of these variations occurs in at least 1% of the population; If 1% is not reached, it is not considered SNP and is a point mutation.
SNPs are distributed heterogeneously throughout the genome and are found in both the coding (exon) and non-coding regions (introns and promoter region) of the genes as well as in the areas of the genome where no known genes settle (sometimes called "junk DNA").