Variant (rsID / SNP)
rs955051
rs955051 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UBASH3B. Location: chromosome 11, position 122,659,918. The table records no clinical significance for this variant.
Reference-table entries
UBASH3BNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 11:122659918
- HGVS
- NM_032873.5,c.882T>G,p.Gly294Gly
- Allele change
- Synonymous_G259G
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
