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. 2021 Jan;9(4):470–477. doi: 10.52547/rbmb.9.4.470

Table 3.

The allele frequency of INSR c.C3174T mutation.

Genotype Number of participants (%) p-value OR (95% CI)
control case
Number (%) Number (%)
CC 57(95) 73(56.2) - 1.0
CT 2(3.3) 56(43.0) 0.00 21.863 (5.116-93.425)
TT 1(2.7) 1(0.8) 0.862 0.781 (0.048- 12.756)
CT+TT 0.00 14.836 (4.417- 49.829)