{{Rsnum
|rsid=104894073
|Chromosome=8
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GATA4
|position=11750213
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GATA4
}}{{omim
|id=600576
|rsnum=104894073
|variant=0001
}}{{ClinVar
|rsid=104894073
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=11607722
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110104
|GENEINFO=GATA4:2626
|GENE_NAME=GATA4
|GENE_ID=2626
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000008.10:g.11607722G>A; NC_000008.10:g.11607722G>C; NC_000008.10:g.11607722G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600576.0001; 600576.0014; 600576.0006
|CLNSIG=5
|CLNCUI=C1842778
|CLNDBN=Atrial septal defect 2; Ventricular septal defect 1
|Disease=Atrial septal defect 2; Ventricular septal defect 1
|CLNACC=RCV000009596.1; RCV000023011.4; RCV000023001.1
|Tags=PM;S3D;OTHERKG;LSD;OM;NOV
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1842778:607941:1478; C3280777:614429:1480
}}