{{Rsnum
|rsid=74315522
|Chromosome=22
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=TBX1
|position=19764224
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TBX1
}}{{omim
|id=602054
|rsnum=74315522
|variant=0005
}}{{ClinVar
|rsid=74315522
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=19751747
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TBX1:6899
|GENE_NAME=TBX1
|GENE_ID=6899
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.19751747C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=602054.0005
|CLNSIG=5
|CLNCUI=C0220704
|CLNDBN=Shprintzen syndrome
|Disease=Shprintzen syndrome
|CLNACC=RCV000008003.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1523:C0220704:192430:567:83092002
}}