Variant (rsID / SNP)
rs2512527
rs2512527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to USP35. Location: chromosome 11, position 77,920,863. The table records no clinical significance for this variant.
Reference-table entries
USP35Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:77920863
- HGVS
- NM_020798.4,c.1962C>A,p.Pro654Pro
- Allele change
- Synonymous_P654P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
