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rs397514629

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514629(C;G)
Make rs397514629(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position113062577
GeneIL36RN
is asnp
is mentioned by
dbSNPrs397514629
ebirs397514629
HLIrs397514629
Exacrs397514629
Varsomers397514629
Maprs397514629
PheGenIrs397514629
hapmaprs397514629
1000 genomesrs397514629
hgdprs397514629
ensemblrs397514629
gopubmedrs397514629
geneviewrs397514629
scholarrs397514629
googlers397514629
pharmgkbrs397514629
gwascentralrs397514629
openSNPrs397514629
23andMers397514629
23andMe allrs397514629
SNP Nexus

SNPshotrs397514629
SNPdbers397514629
MSV3drs397514629
GWAS Ctlgrs397514629
Max Magnitude0
ClinVar
Risk rs397514629(G,T;G,T)
Alt rs397514629(G,T;G,T)
Reference rs397514629(C;C)
Significance Pathogenic
Disease Pustular psoriasis
Variation info
Gene IL36RN
CLNDBN Pustular psoriasis, generalized
Reversed 0
HGVS NC_000002.11:g.113820154C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000033133.5,