Variant (rsID / SNP)
rs1051121
rs1051121 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP1. Location: chromosome 11, position 102,665,973. Clinical significance in the table: Benign.
Reference-table entries
MMP1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:102665973
- Cytoband
- 11q22.2
- HGVS
- NM_002421.4(MMP1):c.831G>A (p.Ala277=)
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.