Variant (rsID / SNP)

rs1503375

rs1503375 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP20. Location: chromosome 9, position 132,623,293. The table records no clinical significance for this variant.

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Reference-table entries

USP20Not classified

Variant type: synonymous_variant
Chromosome / position: 9:132623293
HGVS: NM_001008563.5,c.408C>T,p.Asp136Asp
Allele change: Synonymous_D136D

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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