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rs121913161

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913161(G;T)
Make rs121913161(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position113131068
GeneIL1RN
is asnp
is mentioned by
dbSNPrs121913161
ebirs121913161
HLIrs121913161
Exacrs121913161
Varsomers121913161
Maprs121913161
PheGenIrs121913161
hapmaprs121913161
1000 genomesrs121913161
hgdprs121913161
ensemblrs121913161
gopubmedrs121913161
geneviewrs121913161
scholarrs121913161
googlers121913161
pharmgkbrs121913161
gwascentralrs121913161
openSNPrs121913161
23andMers121913161
23andMe allrs121913161
SNP Nexus

SNPshotrs121913161
SNPdbers121913161
MSV3drs121913161
GWAS Ctlgrs121913161
Max Magnitude0
OMIM147679
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121913161(T;T)
Alt rs121913161(T;T)
Reference rs121913161(G;G)
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.113888645G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015789.25, RCV000084165.1,