Variant (rsID / SNP)

rs35231465

rs35231465 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP8. Location: chromosome 11, position 102,584,135. Clinical significance in the table: Likely benign.

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Reference-table entries

MMP8Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:102584135
Cytoband: 11q22.2
HGVS: NM_002424.3(MMP8):c.1348C>T (p.Gln450Ter)
Allele change: Nonsense_Q427X

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.