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rs2039381

From SNPedia

Orientationminus
Stabilizedplus
Make rs2039381(C;C)
Make rs2039381(C;T)
Make rs2039381(T;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position21481484
GeneIFNE, MIR31HG
is asnp
is mentioned by
dbSNPrs2039381
ebirs2039381
HLIrs2039381
Exacrs2039381
Varsomers2039381
Maprs2039381
PheGenIrs2039381
hapmaprs2039381
1000 genomesrs2039381
hgdprs2039381
ensemblrs2039381
gopubmedrs2039381
geneviewrs2039381
scholarrs2039381
googlers2039381
pharmgkbrs2039381
gwascentralrs2039381
openSNPrs2039381
23andMers2039381
23andMe allrs2039381
SNP Nexus

SNPshotrs2039381
SNPdbers2039381
MSV3drs2039381
GWAS Ctlgrs2039381
GMAF0.06474
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23802172] Association study between nonsense polymorphism (rs2039381, Gln71Stop) of Interferon-ε and susceptibility to vitiligo in Korean population


[PMID 24055696] T Allele of Nonsense Polymorphism (rs2039381, Gln71Stop) of Interferon-ε is a Risk Factor for the Development of Intracerebral Hemorrhage