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Variant (rsID / SNP)

rs1939015

MMP27

rs1939015 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP27. Location: chromosome 11, position 102,576,375. The table records no clinical significance for this variant.

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Reference-table entries

MMP27Not classified
Variant type
missense_variant
Chromosome / position
11:102576375
HGVS
NM_022122.3,c.71C>T,p.Thr24Met
Allele change
Missense_T24M

Public references

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