Variant (rsID / SNP)
rs7201
rs7201 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP2. Location: chromosome 16, position 55,539,614. Clinical significance in the table: Benign.
Reference-table entries
MMP2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 16:55539614
- Cytoband
- 16q12.2
- HGVS
- NM_004530.6(MMP2):c.*260A>C
- Allele change
- Silent
Associated conditions / phenotypes
Multicentric osteolysis, nodulosis, and arthropathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.