Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs117739035
rs117739035
Entrez Id: 59307
Gene Symbol: SIGIRR
SIGIRR
CUI: C4082937
Disease:
Necrotizing enterocolitis in fetus OR newborn
0.010 GeneticVariation BEFREE A forward genetic screen done in an infant with lethal NEC using exome sequencing identified a novel stop mutation (p.Y168X) and a rare missense variant (p.S80Y) in SIGIRR, a gene that inhibits intestinal Toll-like receptor signaling. 25963006 2015
dbSNP: rs766709278
rs766709278
Entrez Id: 59307
Gene Symbol: SIGIRR
SIGIRR
CUI: C4082937
Disease:
Necrotizing enterocolitis in fetus OR newborn
0.010 GeneticVariation BEFREE A forward genetic screen done in an infant with lethal NEC using exome sequencing identified a novel stop mutation (p.Y168X) and a rare missense variant (p.S80Y) in SIGIRR, a gene that inhibits intestinal Toll-like receptor signaling. 25963006 2015
dbSNP: rs7396562
rs7396562
Entrez Id: 59307
Gene Symbol: SIGIRR
SIGIRR
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE In conclusion, our study represents the first report demonstrating an association of the SIGIRR rs7396562</span> polymorphism with SLE susceptibility in a Chinese population. 24826913 2014
dbSNP: rs3210908
rs3210908
Entrez Id: 59307
Gene Symbol: SIGIRR
SIGIRR
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE In addition, we did not find any association between SLE and the rs1152888 IRAK-M (P(meta) (-analysis)  = 0.13) and the rs3210908 SIGIRR (P(meta) (-analysis)  = 0.40) polymorphisms after the meta-analysis. 22634523 2012