{{Rsnum
|rsid=104894383
|Chromosome=12
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TBX5
|position=114403754
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TBX5
}}{{omim
|id=601620
|rsnum=104894383
|variant=0007
}}{{ClinVar
|rsid=104894383
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=114841559
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TBX5:6910
|GENE_NAME=TBX5
|GENE_ID=6910
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.114841559G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601620.0007
|CLNSIG=5
|CLNCUI=C0265264
|CLNDBN=Holt-Oram syndrome
|Disease=Holt-Oram syndrome
|CLNACC=RCV000008461.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1111:C0265264:142900:392:19092004
}}