{{Rsnum
|rsid=387906551
|Chromosome=10
|position=8064140
|Orientation=plus
|geno1=(GCTTACTTCCC;GCTTACTTCCC)
|geno2=(GCTTACTTCCC;T)
|geno3=(T;T)
|Gene=GATA3
|Gene_s=GATA3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=GGCTTACTTCCC
|CHROM=10
|CLNACC=RCV000018108.22
|CLNALLE=1
|CLNDBN=Barakat syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1840333:146255:2237
|CLNHGVS=NC_000010.10:g.8106103delTinsGCTTACTTCCC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=131320.0011
|Disease=Barakat syndrome
|FwdALT=GCTTACTTCCC
|FwdREF=T
|REF=GT
|RSPOS=8106102
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906551
|GENEINFO=GATA3:2625
|GENE_ID=2625
|GENE_NAME=GATA3
}}