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rs397514630

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514630(C;T)
Make rs397514630(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position113059466
GeneIL36RN
is asnp
is mentioned by
dbSNPrs397514630
ebirs397514630
HLIrs397514630
Exacrs397514630
Varsomers397514630
Maprs397514630
PheGenIrs397514630
hapmaprs397514630
1000 genomesrs397514630
hgdprs397514630
ensemblrs397514630
gopubmedrs397514630
geneviewrs397514630
scholarrs397514630
googlers397514630
pharmgkbrs397514630
gwascentralrs397514630
openSNPrs397514630
23andMers397514630
23andMe allrs397514630
SNP Nexus

SNPshotrs397514630
SNPdbers397514630
MSV3drs397514630
GWAS Ctlgrs397514630
Max Magnitude0
ClinVar
Risk rs397514630(T;T)
Alt rs397514630(T;T)
Reference rs397514630(C;C)
Significance Pathogenic
Disease Pustular psoriasis
Variation info
Gene IL36RN
CLNDBN Pustular psoriasis, generalized
Reversed 0
HGVS NC_000002.11:g.113817043C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033134.5,