Variant (rsID / SNP)
rs6933251
rs6933251 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to UST. Location: chromosome 6, position 149,285,138. The table records no clinical significance for this variant.
Reference-table entries
USTNot classified
- Variant type
- intron_variant
- Chromosome / position
- 6:149285138
- HGVS
- NM_005715.3,c.528-408C>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.