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Variant (rsID / SNP)

rs670906

USP2

rs670906 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP2. Location: chromosome 11, position 119,252,199. The table records no clinical significance for this variant.

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Reference-table entries

USP2Not classified
Variant type
missense_variant
Chromosome / position
11:119252199
HGVS
NM_001243759.2,c.29A>C,p.Tyr10Ser
Allele change
Missense_Y10S

Public references

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