Variant (rsID / SNP)

rs5745635

rs5745635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HGF. Location: chromosome 7, position 81,388,042. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

HGFBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 7:81388042
Cytoband: 7q21.11
HGVS: NM_000601.6(HGF):c.333A>G (p.Glu111=)
Allele change: Synonymous_E111E

Associated conditions / phenotypes

Nonsyndromic Hearing Loss, Mixed

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.