Variant (rsID / SNP)

rs16887806

rs16887806 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL21A1. The table records no clinical significance for this variant.

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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.