Nomenclature | SNP | Nucleotide changes | Effect | MAF a | P value for HWF in Controls | |||
---|---|---|---|---|---|---|---|---|
NCBI b | Controls | Cases | P value for association analysis c | |||||
CYP2C19*2 (exon5) | rs4244285 | G681A | Splicing defect | 0.256 | 0.335 | 0.488 | 2.31 × 10-5 | 0.09 |
CYP2C19*3 (exon4) | rs4986893 | G636A | W212X | 0.058 | 0.054 | 0.040 | 0.053 | 0.177 |