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rs387906914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387906914(C;C)
Make rs387906914(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position113060902
GeneIL36RN
is asnp
is mentioned by
dbSNPrs387906914
ebirs387906914
HLIrs387906914
Exacrs387906914
Varsomers387906914
Maprs387906914
PheGenIrs387906914
hapmaprs387906914
1000 genomesrs387906914
hgdprs387906914
ensemblrs387906914
gopubmedrs387906914
geneviewrs387906914
scholarrs387906914
googlers387906914
pharmgkbrs387906914
gwascentralrs387906914
openSNPrs387906914
23andMers387906914
23andMe allrs387906914
SNP Nexus

SNPshotrs387906914
SNPdbers387906914
MSV3drs387906914
GWAS Ctlgrs387906914
Max Magnitude0
ClinVar
Risk rs387906914(C;C)
Alt rs387906914(C;C)
Reference rs387906914(T;T)
Significance Pathogenic
Disease Pustular psoriasis
Variation info
Gene IL36RN
CLNDBN Pustular psoriasis, generalized
Reversed 0
HGVS NC_000002.11:g.113818479T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023446.3,