Variant (rsID / SNP)
rs9835332
rs9835332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TASOR. Location: chromosome 3, position 56,667,682. The table records no clinical significance for this variant.
Reference-table entries
TASORNot classified
- Variant type
- missense_variant
- Chromosome / position
- 3:56667682
- HGVS
- NM_001365635.2,c.3137C>G,p.Thr1046Arg
- Allele change
- Missense_T609R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.