Variant (rsID / SNP)
rs890503
rs890503 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN5. Location: chromosome 15, position 42,150,888. The table records no clinical significance for this variant.
Reference-table entries
SPTBN5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 15:42150888
- HGVS
- NM_016642.4,c.8138C>T,p.Thr2713Ile
- Allele change
- Missense_T2713I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.