Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17006625
rs17006625
KAT2B
0.020 GeneticVariation BEFREE Conversely, the HCC risk was higher in patients with the KAT2B rs17006625 GG (OR = 1.64, 95%CI: 1.01-2.64, P = 0.04). 27350734

2016
dbSNP: rs17006625
rs17006625
KAT2B
0.020 GeneticVariation BEFREE The aim of the current study was to assess the impact of the Ile997Val in EP300 and Asn386Ser in PCAF polymorphisms on the risk of HCC. 22709982

2012