Variant (rsID / SNP)

rs28382575

rs28382575 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP11. Location: chromosome 22, position 24,125,689. The table records no clinical significance for this variant.

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Reference-table entries

MMP11Not classified

Variant type: synonymous_variant
Chromosome / position: 22:24125689
HGVS: NM_005940.5,c.1425T>C,p.Pro475Pro
Allele change: Synonymous_P475P

Associated conditions / phenotypes

Hepatocellular Carcinoma|Cervical Cancer|Cervix Uteri Carcinoma in Situ|Cervical Intraepithelial Neoplasia

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.