{{Rsnum
|rsid=104894722
|Chromosome=19
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TGFB1
|position=41342215
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TGFB1
}}{{omim
|id=190180
|rsnum=104894722
|variant=0005
}}
{{omim
|id=190180
|rsnum=104894722
|variant=0006
}}{{ClinVar
|rsid=104894722
|Reversed=1
|FwdREF=T
|FwdALT=A,C,G
|REF=A
|ALT=C,G,T
|RSPOS=41848120
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050360000000000002110104
|GENEINFO=TGFB1:7040
|GENE_NAME=TGFB1
|GENE_ID=7040
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000019.9:g.41848120A>C; NC_000019.9:g.41848120A>G; NC_000019.9:g.41848120A>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1156; 190180.0006; 190180.0005
|CLNSIG=5
|CLNCUI=C0011989
|CLNDBN=Diaphyseal dysplasia
|Disease=Diaphyseal dysplasia
|CLNACC=RCV000013356.23; RCV000013359.23; RCV000032151.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1156:C0011989:131300:1328:34643004
}}