IRF7, interferon regulatory factor 7, 3665

N. diseases: 121; N. variants: 11
Disease: Thyroid associated opthalmopathies ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1061501
rs1061501
Entrez Id: 3665
Gene Symbol: IRF7
IRF7
CUI: C0339143
Disease:
Thyroid associated opthalmopathies 		0.010 GeneticVariation BEFREE Furthermore, the allele G frequency of rs1061501 was associated with Graves' ophthalmopathy (<i>P</i> = 0.035, OR = 1.396). 30774658 2019