Gene entry

TFAM

transcription factor A, mitochondrial

Chromosome: 10
Cytoband: 10q21.1
Variants (rsID): 7

TFAM is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q21.1). Its official name is “transcription factor A, mitochondrial”. The reference table lists 7 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs757075712Likely pathogenicsingle nucleotide variantMitochondrial DNA depletion syndrome, hepatocerebral form|Mitochondrial DNA depletion syndrome 15 (hepatocerebral type)

Other listed variants

rs1049432
rs10826179
rs16912197
rs41307508
rs74827573
rs117669234

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.