Variant (rsID / SNP)
rs3765620
rs3765620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP8. Location: chromosome 11, position 102,595,492. Clinical significance in the table: Benign.
Reference-table entries
MMP8Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:102595492
- Cytoband
- 11q22.2
- HGVS
- NM_002424.3(MMP8):c.95C>T (p.Thr32Ile)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.