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Variant (rsID / SNP)

rs75370284

USP35

rs75370284 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP35. Location: chromosome 11, position 77,921,348. The table records no clinical significance for this variant.

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Reference-table entries

USP35Not classified
Variant type
missense_variant
Chromosome / position
11:77921348
HGVS
NM_020798.4,c.2447G>A,p.Arg816His
Allele change
Missense_R816H

Public references

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