Variant (rsID / SNP)
rs118052277
rs118052277 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP28. Location: chromosome 17, position 34,093,597. The table records no clinical significance for this variant.
Reference-table entries
MMP28Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:34093597
- HGVS
- NM_024302.5,c.1482A>G,p.Ala494Ala
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.