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Characteristically, we detected various polymorphisms within the same intergenic regions isolated from individual clones.
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We first examined the relative co-occurrence of the various polymorphisms at the sample level and at the population level.
Various polymorphisms in these genes are summarized in Table 2.
Various studies have assessed associations between various polymorphisms in the VDR gene and breast cancer risk, with inconsistent results.
Given these observations, we investigated the relationship of several known and novel polymorphisms within GATA2 to coronary artery disease.
This finding initiated a series of reports in various populations confirming the effect of these polymorphisms within the TCF7L2 gene on the type 2 diabetes risk [ 4– 12].
This can be done at various levels by comparing the genome organization, the gene repertoire and the polymorphisms within the genes.
In GWAS, variations (polymorphisms) within the genomic DNA nucleotide sequences of individuals are studied for their statistical associations with various diseases or disease traits.
Different STs as well as a number of additional genetic polymorphisms within this strain might suggest a polyphyletic origin by multiple and independent transfers of SCCmec II elements to various CC5-MSSA precursor strains [46].
And that is that our goal is to look at polymorphisms within the fragment.
SnpEff annotated polymorphisms within 32,410 and 31,119 genic regions in A. halleri-derived and A. lyrata-derived genomes, respectively.
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