Variant (rsID / SNP)
rs117651561
rs117651561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP28. Location: chromosome 17, position 34,093,663. The table records no clinical significance for this variant.
Reference-table entries
MMP28Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 17:34093663
- HGVS
- NM_024302.5,c.1416C>T,p.Pro472Pro
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.