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Variant (rsID / SNP)

rs3744793

USP36

rs3744793 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP36. Location: chromosome 17, position 76,817,090. The table records no clinical significance for this variant.

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Reference-table entries

USP36Not classified
Variant type
missense_variant
Chromosome / position
17:76817090
HGVS
NM_001385169.1,c.811G>A,p.Val271Ile
Allele change
Missense_V271I

Public references

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