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Variant (rsID / SNP)

rs587985

USP2

rs587985 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP2. Location: chromosome 11, position 119,244,095. The table records no clinical significance for this variant.

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Reference-table entries

USP2Not classified
Variant type
synonymous_variant
Chromosome / position
11:119244095
HGVS
NM_004205.5,c.96G>A,p.Pro32Pro
Allele change
Silent

Public references

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