TABLE 2.
Genotype | P value | Significanceb |
---|---|---|
Pfnhe-1 ms4760 profiles | 0.0021 | S |
Pfnhe-1, no. of DNNND repeats | 0.0007 | S |
Pfnhe-1, no. of NHNDNHNNDDD repeats | 0.0020 | S |
Mutation in codon 74 of Pfcrt gene | 0.0454 | NS |
Mutation in codon 75 of Pfcrt gene | 0.0454 | NS |
Mutation in codon 76 of Pfcrt gene | 0.0454 | NS |
Mutation in codon 220 of Pfcrt gene | 0.0454 | NS |
Mutation in codon 271 of Pfcrt gene | 0.0688 | NS |
Mutation in codon 326 of Pfcrt gene | 0.0019 | S |
Mutation in codon 356 of Pfcrt gene | 0.0687 | NS |
Mutation in codon 371 of Pfcrt gene | 0.0454 | NS |
Mutation in codon 86 of Pfmdr1 gene | 1.0000 | NS |
Mutation in codon 184 of Pfmdr1 gene | 0.5754 | NS |
Mutation in codon 1034 of Pfmdr1 gene | 0.0119 | NS |
Mutation in codon 1042 of Pfmdr1 gene | 0.0119 | NS |
Mutation in codon 1246 of Pfmdr1 gene | 0.5228 | NS |
Mutation in codon 191 of Pfmrp gene | 0.0036 | NS |
Mutation in codon 437 of Pfmrp gene | 0.0036 | NS |
Determined by Mann-Whitney U test or Kruskal-Wallis test. The variable was the QN IC50. The significance cutoff was 0.0028 (0.05/18, 18 tests, Bonferroni correction).
S, significant; NS, nonsignificant.