Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10069690
rs10069690
TERT
0.010 GeneticVariation BEFREE We found that rs10069690</span> was significantly associated with an increased CHB risk in the dominant model (adjusted OR = 1.70, 95% CI: 1.06-2.71, <i>P</i> = 0.031) and additive model (adjusted OR = 1.62, 95% CI: 1.09-2.41, <i>P</i> = 0.018). 29507683

2018