Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1143634
rs1143634
IL1B
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.020 GeneticVariation BEFREE Also in the exon 5 (rs1143634), a significant increase in frequency of the C/C homozygous genotype (P = 0.001; OR = 0.18, 95% CI = 0.11-0.30) and C allele (P = 0.001; OR = 0.31, 95% CI = 0.20-0.48) was observed in GD cases as against controls. 29454070

2018
dbSNP: rs1143634
rs1143634
IL1B
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.020 GeneticVariation BEFREE In the IL1B SNPs examined, the C allele of rs1143634 was associated with GD, whereas the T/T genotype of the SNPs rs1143634 and rs16944 were less associated with the disease. 20671275

2010