Gene entry

TGFB1

transforming growth factor beta 1

Chromosome: 19
Cytoband: 19q13.2
Variants (rsID): 13

TGFB1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.2). Its official name is “transforming growth factor beta 1”. The reference table lists 13 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

rs1800470Benignsingle nucleotide variantBreast cancer, invasive, susceptibility to|Cystic fibrosis|Inflammatory bowel disease, immunodeficiency, and encephalopathy|Diaphyseal dysplasia
rs1800471Benignsingle nucleotide variant
rs1800472Benignsingle nucleotide variant

Other listed variants

rs1800469
rs2241716
rs4803455
rs8110090
rs13306709
rs111403414
rs186051435
rs189709530
rs190566789
rs199982059

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.