Variant (rsID / SNP)
rs679620
rs679620 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP3. Location: chromosome 11, position 102,713,620. Clinical significance in the table: Benign.
Reference-table entries
MMP3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:102713620
- Cytoband
- 11q22.2
- HGVS
- NM_002422.5(MMP3):c.133A>G (p.Lys45Glu)
- Allele change
- Missense_K45E
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.