Table 2.
Sequence change | Classification of change | Alteration in amino acid sequence | Frequency of SNP in patients | Frequency of SNP in controls | Fisher’s exact test | |||
---|---|---|---|---|---|---|---|---|
Allele (%) | Genotype (%) | Allele (%) | Genotype (%) | AlleleP | GenotypeP | |||
Exon7 C(1038)G | SNP1 | Missense Thr→Ser | 1/35 (2.8%) | C/G 1/18(5.5%) | 1/199 (0.50%) | C/G 1/99 (1.01%) | 0.282 | 0.282 |