{{Rsnum
|rsid=137853322
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=IKBKG
|position=154564420
|Gene_s=IKBKG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300248
|variant=0005
|rsnum=137853322
}}{{ClinVar
|rsid=137853322
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=153792635
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=IKBKG:8517
|GENE_NAME=IKBKG
|GENE_ID=8517
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.153792635A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300248.0005
|CLNSIG=5
|CLNCUI=C0021171
|CLNDBN=Incontinentia pigmenti syndrome
|Disease=Incontinentia pigmenti syndrome
|CLNACC=RCV000012202.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1472:C0021171:308300:464:367520004
}}