Table 5.
Genotype and allele frequencies for rs6977848, rs66461782, and rs12940701 in study vs. HapMap/1000 genomes data.
| p-Value | Genotyping result | HapMap/1000 genome | |||
|---|---|---|---|---|---|
| miR-148a | rs6977848 | G T |
0.56 (non-significant) | 38.5% 61.5% |
42.5% 57.5% |
| GG GT TT |
0.34 (non-significant) | 15.7% 45.6% 38.7% |
23.3% 38.3% 38.3% |
||
| miR-186 | rs66461782 | A T |
0.66 (non-significant) | 79.1% 20.9% |
76.5% 23.5% |
| AA AT TT |
0.56 (non-significant) | 62.0% 34.2% 3.7% |
60.0% 32.9% 7.1% |
||
| miR-152 | rs12940701 | C T |
0.34 (non-significant) | 66.8% 33.2% |
72.9% 27.1% |
| CC CT TT |
0.23 (non-significant) | 42.4% 48.8% 8.8% |
54.1% 37.6% 8.3% |
Data from http://www.ncbi.nlm.nih.gov and http://www.ensembl.org/index.html.