Gene entry
HGF
hepatocyte growth factor
- Chromosome
- 7
- Cytoband
- 7q21.11
- Variants (rsID)
- 22
HGF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q21.11). Its official name is “hepatocyte growth factor”. The reference table lists 22 variants (rsID) for this gene.
Clinically classified variants
6 reference-table entries with clinical significance.
- rs5745635Benignsingle nucleotide variantNonsyndromic Hearing Loss, Mixed
- rs5745687Benignsingle nucleotide variantNonsyndromic Hearing Loss, Mixed
- rs142045938Conflicting interpretationssingle nucleotide variantNonsyndromic Hearing Loss, Mixed
- rs145494248Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 39
- rs145598174Conflicting interpretationssingle nucleotide variant
- rs147075806Conflicting interpretationssingle nucleotide variant
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.