Result: The crude ORs for
A799G,
A987G and
T1055A were 3.37 (95% CI: 1.17-9.67), 6.08 (95%CI: 1.31-28.19) and 4.45 (95% CI: 1.72-11.54), respectively.
Discussion: We found that the mutations
A799G,
A987G, and
T1055A were detectable in >75% patients (3 of 4 patients for
A799G, 2 of 2 patients for
A987G, and 4 of 5 patients for
T1055A) 4-5 years before the clinical diagnosis of
HCC (Table S3 in File S1).