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Variant (rsID / SNP)

rs2271928

COL16A1

rs2271928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to COL16A1. Location: chromosome 1, position 32,127,953. The table records no clinical significance for this variant.

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Reference-table entries

COL16A1Not classified
Variant type
synonymous_variant
Chromosome / position
1:32127953
HGVS
NM_001856.4,c.3663C>T,p.Asp1221Asp
Allele change
Synonymous_D1221D

Public references

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