{{Rsnum
|rsid=2241715
|Gene=TGFB1
|Chromosome=19
|position=41350981
|Orientation=minus
|GMAF=0.3705
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=TGFB1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 54.0 | 35.4 | 10.6
| HCB | 28.7 | 46.3 | 25.0
| JPT | 29.5 | 50.0 | 20.5
| YRI | 52.4 | 35.9 | 11.7
| ASW | 56.1 | 36.8 | 7.0
| CHB | 28.7 | 46.3 | 25.0
| CHD | 20.6 | 41.1 | 38.3
| GIH | 38.6 | 43.6 | 17.8
| LWK | 51.4 | 39.4 | 9.2
| MEX | 36.8 | 49.1 | 14.0
| MKK | 52.6 | 38.5 | 9.0
| TSI | 37.6 | 42.6 | 19.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=19258388
|Title=Genetic variation in the transforming growth factor-{beta}1 gene is associated with susceptibility to IgA nephropathy.
|OA=1
}}

{{PMID Auto
|PMID=19910030
|Title=Evaluation of candidate genes in a genome-wide association study of childhood asthma in Mexicans
|OA=1
}}

{{PMID Auto
|PMID=18292811
|Title=Complex two-gene modulation of lung disease severity in children with cystic fibrosis.
|OA=1
}}

{{PMID Auto
|PMID=20479942
|Title=Genetic risk factors in lupus nephritis and IgA nephropathy--no support of an overlap.
|OA=1
}}

{{ClinVar
|ALT=C
|CAF=0.3705; 0.6295
|CHROM=19
|CLNACC=RCV000032145.1
|CLNALLE=1
|CLNDBN=Diaphyseal dysplasia
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1156:C0011989:131300:1328:34643004
|CLNHGVS=NC_000019.9:g.41856886A>C
|CLNSIG=2
|CLNSRC=GeneReviews
|CLNSRCID=NBK1156
|COMMON=1
|Disease=Diaphyseal dysplasia
|FwdALT=G
|FwdREF=T
|GENEINFO=TGFB1:7040
|GENE_ID=7040
|GENE_NAME=TGFB1
|REF=A
|RSPOS=41856886
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;VLD;G5A;G5;HD;GNO;KGPhase1;KGPilot123;KGPROD;OTHERKG;PH3;LSD
|VC=SNV
|VP=0x05016800000017051f100100
|WGT=0
|dbSNPBuildID=98
|rsid=2241715
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}