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Variant (rsID / SNP)

rs10083789

USP31

rs10083789 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP31. Location: chromosome 16, position 23,080,634. The table records no clinical significance for this variant.

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Reference-table entries

USP31Not classified
Variant type
missense_variant
Chromosome / position
16:23080634
HGVS
NM_020718.4,c.2792G>T,p.Arg931Leu
Allele change
Missense_R931L

Public references

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