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

Table 5.

The allele frequency of FSHR c.A2039G mutation.

Genotype Number of participants (%) p-value OR (95% CI)
control case
Number (%) Number (%)
AA 53(88.3) 68(56.7) - 1.0
AG 6(10) 43(35.8) 0.000 5.586 (2.211-14.109)
GG 1(1.7) 9(7.5) 0.037 7.015 (0.862-57.110)
AG+GG 7(11.7) 52(43.3) 0.000 5.790 (2.433- 13.778)