Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
Selective immunoglobulin A deficiency 		0.130 GeneticVariation GWASCAT Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. 27723758

2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
Selective immunoglobulin A deficiency 		0.130 GeneticVariation BEFREE Our genome-wide association study (GWAS) meta-analysis of 1,635 patients with IgAD and 4,852 controls identified four new significant (P < 5 × 10<sup>-8</sup>) loci and association with a rare IFIH1 variant (p.Ile923Val). 27723758

2016
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
Selective immunoglobulin A deficiency 		0.130 GeneticVariation BEFREE Brief Report: IFIH1 Mutation Causes Systemic Lupus Erythematosus With Selective IgA Deficiency. 25777993

2015
Entrez Id: 64135
Gene Symbol: IFIH1
IFIH1
CUI: C4049006
Disease: Selective immunoglobulin A deficiency
Selective immunoglobulin A deficiency 		0.130 GeneticVariation BEFREE Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. 20694011

2010