Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1861494
rs1861494
IFNG ; IFNG-AS1
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		0.010 GeneticVariation BEFREE The <i>IFNG</i> rs1861494 was significantly associated with LTBI in recessive model, and the CC+CT genotype decreased risk of LTBI by 50% (<i>P</i> = 0.046, OR = 0.50, 95%CI: 0.25-0.99). 31687049

2019