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rs137853332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853332(A;A)
Make rs137853332(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154563602
GeneIKBKG
is asnp
is mentioned by
dbSNPrs137853332
ebirs137853332
HLIrs137853332
Exacrs137853332
Varsomers137853332
Maprs137853332
PheGenIrs137853332
hapmaprs137853332
1000 genomesrs137853332
hgdprs137853332
ensemblrs137853332
gopubmedrs137853332
geneviewrs137853332
scholarrs137853332
googlers137853332
pharmgkbrs137853332
gwascentralrs137853332
openSNPrs137853332
23andMers137853332
23andMe allrs137853332
SNP Nexus

SNPshotrs137853332
SNPdbers137853332
MSV3drs137853332
GWAS Ctlgrs137853332
Max Magnitude0
OMIM300248
Desc
Variant0022
Relatedalso
ClinVar
Risk rs137853332(A;A)
Alt rs137853332(A;A)
Reference rs137853332(G;G)
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.153791817G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000012223.3,