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Variant (rsID / SNP)

rs2499953

MMP26

rs2499953 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MMP26. Location: chromosome 11, position 5,010,905. The table records no clinical significance for this variant.

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Reference-table entries

MMP26Not classified
Variant type
missense_variant
Chromosome / position
11:5010905
HGVS
NM_021801.5,c.127A>G,p.Lys43Glu
Allele change
Missense_K43E

Associated conditions / phenotypes

Kawasaki Disease

Public references

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