{{Rsnum
|rsid = 28939668
|Gene = JAG1
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=20
|position=10652533
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=JAG1
}}{{omim
|desc=TETRALOGY OF FALLOT
|id=601920
|rsnum=28939668
|variant=0010
}}{{ClinVar
|rsid=28939668
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=10633181
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=JAG1:182
|GENE_NAME=JAG1
|GENE_ID=182
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.10633181C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601920.0010
|CLNSIG=5
|CLNCUI=C0039685
|CLNDBN=Tetralogy of Fallot
|Disease=Tetralogy of Fallot
|CLNACC=RCV000008063.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0039685:187500:3303:86299006
}}