Gene entry

TGFBI

transforming growth factor beta induced

Chromosome: 5
Cytoband: 5q31.1
Variants (rsID): 12

TGFBI is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q31.1). Its official name is “transforming growth factor beta induced”. The reference table lists 12 variants (rsID) for this gene.

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Clinically classified variants

3 reference-table entries with clinical significance.

rs148555720Benignsingle nucleotide variantCorneal dystrophy
rs267607109Othersingle nucleotide variantCorneal Dystrophy, Lattice Type I
rs267607110Othersingle nucleotide variantCorneal Dystrophy, Lattice Type I

Other listed variants

rs2302037
rs11242307
rs17169726
rs45613531
rs73296968
rs182124708
rs184978714
rs199686929
rs757860567

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.