38. In the human genome, a variation in a single DNA base pair, such as the substitution of a cytosine ( C ) for a thymine (T), that occurs in more than 1% of the population is known as a __________. They serve as powerful molecular markers in genome-wide association studies (GWAS) to identify genetic predispositions to complex diseases.
(A) insertion-deletion mutation (InDel)
(B) haplotype block
(C) single nucleotide polymorphism (SNP)
(D) copy number variant (CNV)
(E) short tandem repeat (STR)

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統計: A(0), B(0), C(1), D(0), E(0) #3853343