Gene: IL18 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs187238
rs187238
IL18
0.010 GeneticVariation BEFREE The frequency of the C/G genotype of rs187238 was significantly higher in patients and conferred a risk of HT (OR, 1.96; 95% CI, 1.30-2.95; Pc, 0.0021). 23073298

2013
dbSNP: rs1946518
rs1946518
IL18
0.010 GeneticVariation BEFREE There was no association between HT and rs1946518. 23073298

2013