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Variant (rsID / SNP)

rs2160276

CES5A

rs2160276 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CES5A. Location: chromosome 16, position 55,883,618. The table records no clinical significance for this variant.

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Reference-table entries

CES5ANot classified
Variant type
synonymous_variant
Chromosome / position
16:55883618
HGVS
NM_001190158.1,c.1428A>G,p.Pro476Pro
Allele change
Silent

Public references

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