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rs137853331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853331(A;C)
Make rs137853331(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154563590
GeneIKBKG
is asnp
is mentioned by
dbSNPrs137853331
ebirs137853331
HLIrs137853331
Exacrs137853331
Varsomers137853331
Maprs137853331
PheGenIrs137853331
hapmaprs137853331
1000 genomesrs137853331
hgdprs137853331
ensemblrs137853331
gopubmedrs137853331
geneviewrs137853331
scholarrs137853331
googlers137853331
pharmgkbrs137853331
gwascentralrs137853331
openSNPrs137853331
23andMers137853331
23andMe allrs137853331
SNP Nexus

SNPshotrs137853331
SNPdbers137853331
MSV3drs137853331
GWAS Ctlgrs137853331
Max Magnitude0
OMIM300248
Desc
Variant0021
Relatedalso
ClinVar
Risk rs137853331(C;C)
Alt rs137853331(C;C)
Reference rs137853331(A;A)
Significance Pathogenic
Disease Familial atypical mycobacteriosis
Variation info
Gene IKBKG
CLNDBN Familial atypical mycobacteriosis, type 1, X-linked
Reversed 0
HGVS NC_000023.10:g.153791805A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000012222.3,