Variant (rsID / SNP)
rs12708402
rs12708402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPTBN5. Location: chromosome 15, position 42,171,462. The table records no clinical significance for this variant.
Reference-table entries
SPTBN5Not classified
- Variant type
- missense_variant
- Chromosome / position
- 15:42171462
- HGVS
- NM_016642.4,c.3178G>A,p.Val1060Ile
- Allele change
- Missense_V1060I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.