Variant (rsID / SNP)
rs2270587
rs2270587 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSPAN8. Location: chromosome 12, position 71,526,593. The table records no clinical significance for this variant.
Reference-table entries
TSPAN8Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 12:71526593
- HGVS
- NM_001369760.1,c.456C>T,p.Cys152Cys
- Allele change
- Synonymous_C152C
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.