Variant (rsID / SNP)
rs79742527
rs79742527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP28. Location: chromosome 17, position 34,093,681. The table records no clinical significance for this variant.
Reference-table entries
MMP28Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:34093681
- HGVS
- NM_024302.5,c.1398C>T,p.Ser466Ser
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.