Variant (rsID / SNP)
rs5745687
rs5745687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HGF. Location: chromosome 7, position 81,359,051. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
HGFBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:81359051
- Cytoband
- 7q21.11
- HGVS
- NM_000601.6(HGF):c.910G>A (p.Glu304Lys)
- Allele change
- Missense_E304K
Associated conditions / phenotypes
Nonsyndromic Hearing Loss, Mixed
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.