Interestingly, the 4.3″ display on AT&T's variant is smaller than the 4.52 incher found on both Sprint and T-Mobile, but AT&T's model is also the slimmest of the lot (at 8.89mm).
For both candidate and GWAS identified SNPs the risks conferred by any one gene variant are small to modest (OR = 1.2 1.5) and cannot be used to effectively determine risk.
This should be expected, however, as the recruitment was not based on genotype, and because of this the numbers with the TT variant were small (supplement n=3, placebo n=4).
GWAS have successfully located genetic variants for medical and psychiatric disorders [1] [7], but the variance explained collectively by these genetic variants is small compared to the heritability estimates obtained in family studies.
Although many pathological mutations have been identified [17], [18], the number of such variants is small compared to the number of known polymorphisms, and it is still unclear which polymorphisms have biological effects.
Compared with germline results, the agreement of the identified variants is small (depicted in Figure 2B).
The clinical relevance of identified genetic variants for predicting risk of endometriosis is unclear because the overall increase in risk caused by the known variants is small [ 70].
However, the effect of the different variants is small, and analysis of the β-cell responsiveness to the incretin hormones is technically demanding.
