Table 2.
SNP | Recessive allele (frequency)* |
Association with pT0† | Association with <pT2 (downstaging)‡ |
||
---|---|---|---|---|---|
OR | P value | OR | P value | ||
rs10964552 | A (0.13) | NA | NA | 0.20 | 0.017 |
rs1649942 | C (0.20) | 0.00 | 0.994 | 1.02 | 0.963 |
rs2136241 | C (0.46) | 0.82 | 0.795 | 1.08 | 0.832 |
rs2191934 | T (0.47) | 0.42 | 0.300 | 1.26 | 0.535 |
rs244898 | T (0.41) | 6.82 | 0.006 | 1.60 | 0.192 |
rs3893319 | G (0.05) | NA | NA | 1.93 | 0.471 |
rs6870861 | C (0.11) | 0.00 | 0.992 | 0.38 | 0.131 |
rs7937567 | G (0.38) | 4.75 | 0.040 | 0.95 | 0.885 |
rs9527419 | T (0.14) | NA | NA | 1.09 | 0.871 |
allele frequency in the discovery cohort of this study
OR= odds ratio
using recessive genetic model. OR are calculated using the major allele as the reference (comparator). NA: for these results, OR and P values are not provided since these were test instances where there were either zero or only one homozygous recessive patient present in the cohort. OR and P values for these situations in a recessive model were therefore undependable.
using additive genetic model; the OR is expressed for the impact of carriage of increasing copies of the minor allele