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rs121913162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913162(C;T)
Make rs121913162(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position113129619
GeneIL1RN
is asnp
is mentioned by
dbSNPrs121913162
ebirs121913162
HLIrs121913162
Exacrs121913162
Varsomers121913162
Maprs121913162
PheGenIrs121913162
hapmaprs121913162
1000 genomesrs121913162
hgdprs121913162
ensemblrs121913162
gopubmedrs121913162
geneviewrs121913162
scholarrs121913162
googlers121913162
pharmgkbrs121913162
gwascentralrs121913162
openSNPrs121913162
23andMers121913162
23andMe allrs121913162
SNP Nexus

SNPshotrs121913162
SNPdbers121913162
MSV3drs121913162
GWAS Ctlgrs121913162
Max Magnitude0
OMIM147679
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121913162(T;T)
Alt rs121913162(T;T)
Reference rs121913162(C;C)
Significance Pathogenic
Disease Osteomyelitis not provided
Variation info
Gene IL1RN
CLNDBN Osteomyelitis, sterile multifocal, with periostitis and pustulosis not provided
Reversed 0
HGVS NC_000002.11:g.113887196C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015790.25, RCV000084164.1,