{{Rsnum
|rsid=113994138
|Chromosome=17
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GTG)
|geno3=(GTG;GTG)
|Gene=STAT3
|position=42325038
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=STAT3
}}{{omim
|id=102582
|rsnum=113994138
|variant=0001
}}{{ClinVar
|rsid=113994138
|Reversed=1
|FwdREF=GTG
|FwdALT=
|REF=TCAC
|ALT=T
|RSPOS=40477055
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110200
|GENEINFO=STAT3:6774
|GENE_NAME=STAT3
|GENE_ID=6774
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.40477056_40477058delCAC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK25507; 102582.0001
|CLNSIG=5
|CLNCUI=C0022398; C0022398
|CLNDBN=Hyperimmunoglobulin E syndrome
|Disease=Hyperimmunoglobulin E syndrome
|CLNACC=RCV000019965.26
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK25507:C0022398:147060:2314:50926003
}}