{{Rsnum
|rsid=104894165
|Chromosome=10
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=GATA3
|position=8073747
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GATA3
}}{{omim
|id=131320
|rsnum=104894165
|variant=0012
}}{{ClinVar
|rsid=104894165
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=8115710
|CHROM=10
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GATA3:2625
|GENE_NAME=GATA3
|GENE_ID=2625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.8115710A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=131320.0012
|CLNSIG=5
|CLNCUI=C1840333
|CLNDBN=Barakat syndrome
|Disease=Barakat syndrome
|CLNACC=RCV000018109.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1840333:146255:2237
}}