IFNE, interferon epsilon, 338376

N. diseases: 12; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2039381
rs2039381
Entrez Id: 338376;554202
Gene Symbol: IFNE;MIR31HG
IFNE;MIR31HG
CUI: C1274648
Disease:
Segmental vitiligo
0.010 GeneticVariation BEFREE This study suggests that rs2039381 (Gln71Stop) polymorphism of IFNE may be related to onset time of vitiligo in NSV</span> patients. 23802172 2013