I must apologize and withdraw my challenge.
Polymorphisms (genetic variation) associated with disease
are termed mutations.
Natural DNA variation is termed a "genetic polymorphism."
There is no language for "positive genetic mutations" likely because no clear examples exist.
There can be no "Positive Mutations" by definition.
So to ask for such is not a fair request.
I could change the challenge to ask for "Positive DNA Variants" but since variation is a positive aspect itself, that would serve no purpose.
I'm afraid you and your source are both pretty confused about the terminology here. "Polymorphism" means a genetic variant, sometimes with the restriction that it occur above some frequency in the population, sometimes without that restriction.(*) Whether a variant is termed a mutation or not has nothing to do with whether it's associated with disease (look, for example, at any of the many genome-wide association studies that have been performed in the last few years -- they may use "variant" or they may use "polymorphism", but they don't use "mutation"). A mutation is a change to DNA; all the mutations we're talking about here are germ-line mutations, that is, mutations that are passed down to descendants.
As soon as a mutation has occurred, what you have is a new genetic variant. If you're interested in the fact that it is a change compared to some previous state, you might keep referring to it as a mutation in later generations, but that's kind of sloppy terminology (even though I use it myself).
The term for "positive mutation" is "beneficial mutation", and the term for "positive DNA variant" is "beneficial allele". A beneficial mutation, by definition, produces a beneficial allele.
Each human acquires roughly 70 mutations when he or she is born, i.e. 70 new genetic variants, added to ~4 million inherited variants. If you compare new mutations with existing variants, the existing variants turn out to look exactly like a whole lot of new mutations that have accumulated and spread in the population over many hundreds of thousands of years -- the same distribution of types of mutations (transitions, transversions, CpGs, insertions and deletions), with the expected frequency spectrum. So the strong evidence is that existing variation really is nothing but the result of a whole lot of mutation. If someone wants to argue otherwise, they're going to have to present some evidence.
(*) The authors of the HapMap 3 paper, for example, just had a long-running debate about whether "polymorphism" should be restricted to variants above some frequency, should include all frequencies, or should be dropped entirely. In the end, we dropped the term except when defining SNPs and CNPs (single-nucleotide and copy-number polymorphisms, respectively).